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A special thank you to Paul Kennedy of Co. Clare, Ireland, for invaluable information.

References

[1] Ishihara M, Tsuneya T and Uneyama K. Fragrant Sesquiterpenes from Agarwood.
Phytochemistry 1993;33:1147-1155.

[2] Johnson P. Die Anvendung der Headspace-Erkenntniss in der Kreation. Parfümerie Kosmetik 1987;68(6):356-357.

[3] Ohloff G. Scent and Fragrances. The Fascination of Odors and their Chemical Perspectives. Berlin, Heidelberg: Springer-Verlag; 1994.

[4] Tamogami S et al. Analysis of enantiomeric ratios of aroma components in several flowers using a Chiramix column. Flavour Fragr J 2004;19:1-5.

[5] Müller PM, Lamparsky D. Perfumes: Art, Science & Technology. Amsterdam, New York: Elsevier; 1991.

[6] Bauer K, Garbe D, Surburg H. Common fragrance and flavor materials: preparation, properties and uses. 2nd ed. Weinheim: VCH; 1990. OBS: A newer edition is available, see ref. [146].

[7] Svoboda KP et al. Biomass production, essential oil yield and composition of Myrica gale L. harvested from wild populations in Scotland and Finland. Flavour Fragr J 1998;13:367-372.

[8] Mookherje BD et al. The chemistry of flowers, fruits and spices: live versus dead - a new dimension in fragrance research. Pure Appl Chem 1990;62(7):1357-1364.

[9] Lamparsky D. Headspace technique as a versatile complementary tool to increase knowledge about constituents of domestic or exotic flowers and fruits. In: Baerheim Svendsen A, Scheffer JJC, editors. Essential Oils and Aromatic Plants. Proceedings of the 15th International Symposium on Essential Oils. Dordrecht: Martinus Nijhoff / Dr. W. Junk Publishers; 1985; 79-92.

[10] Fleischmann P, Watanabe N, Winterhalter P. Enzymatic carotenoid cleavage in star fruit (Averrhoa carambola). Phytochemistry 2003;63(2):131-7.

[11] Macleod G, Ames JM. Volatile components of starfruit. Phytochemistry 1990;29(1):165-172.

[12] Andersson S, Nilsson LA, Groth I, Bergström G. Floral scents in butterfly-pollinated plants: possible convergence in chemical composition. Botanical Journal of the Linnean Society 2002;140:129-153.

[13] Andersson S. Antennal responses to floral scents in the butterflies Inachis io, Aglais urticae (Nymphalidae), and Gonepteryx rhamni (Pieridae). Chemoecology 2003;13:13-20.

[14] South African National Biodiversity Institute, February 2005. www.plantzafrica.com

[15] Illy E. The complexity of coffee. Scientific American 2002;286(6):72-77.

[16] Buffo RA, Cardelli-Freire C. Coffe flavour: an overview. Flavour Fragr J 2004;19:99-104.

[17] Elss S et al. Aroma profile of pineapple (Ananas comosus) and pineapple products. LTW - Food Science and Technology 2005;38:263-274.

[18] Miyazawa M, Yamafuji C. Inhibition of acetylcholinesterase activity by tea tree oil and constituent terpenoids. Flavour Fragr J 2005 (In press).

[19] Hausen BM, Reichling J, Harkenthal M. Degradation products of monoterpenes are the sensitizing agents in tea tree oil. Am J Contact Dermat 1999;10(2):68-77.

[20] Bernhard Weber, Birgit Maas, and Armin Mosandl. Stereoisomeric Flavor Compounds. 72. Stereoisomeric Distribution of Some Chiral Sulfur-Containing Trace Components of Yellow Passion Fruits. J Agric Food Chem 1995;43: 2438-2441.

[21] Yolka S et al. gamma-Sultines: a new class of flavour compounds. Flavour Fragr J 2002;17: 425–431.

[22] Robertson GW et al. A comparison of the flower volatiles from hawthorn and four raspberry cultivars. Phytochemistry 1993;33(5):1047-1053.

[23] Mahattanatawee K, Goodner KL, Baldwin EA. Determination of aroma active volatiles In Florida tropical fruit by GC-O And GC-MS. American Chemical Society National Meeting. Paper No. Agfd 19, 2005.

[24] Jirovetz L et al. Analysis of the essential oils of the leaves, stems, rhizomes and roots of the medicinal plant Alpinia galanga from southern India. Acta Pharm 2003;53:73-81.

[25] Couladis M et al. Essential oil of Salvia officinalis from Serbia and Montenegro. Flavour Fragr J 2002;17:119-126.

[26] Miranda EJF, Nogueira RI, Pontes SM, Rezende CM. Odour-active compounds of banana passa identified by aroma extract dilution analysis. Flavour Fragr J 2001;16:281-285.

[27] Naef R, Jaquier A, Velluz A, Bachofen B. From the linden flower to linden honey - volatile constituents of linden nectar, the extract of bee-stomach and ripe honey. Chemistry and Biodiversity 2004;1:1870-1879.

[28] Porter AEA, Griffiths DW, Robertson GW, Sexton R. Floral volatiles of the sweet pea Lathyrus odoratus. Phytochemistry 1999;51:211-214.

[29] Key odorants in strawberry flavor. Annual Report 1996. Deutsche Forschungsanstalt für Lebensmittelchemie, Lichtenbergstr. 4, D-85748 Garching.

[30] Talon T, Raynaud C, Gaset A. Black truffle odor key-compounds identification based on hunting animals and human expert olfactory evaluation. Paper presented at 'Advances in Semiochemistry 2000', Brighton 20th-24th July, 2000.

[31] Hisano H, Ishimaru K, Tada H, Ikeda Y. Flavors of heliotrope flowers, analyzed by solid phase microextraction method. Saga Prefectural Institute of Public Health, 1-20 Hatchounawate-machi, Saga City 849, Japan, 1995.

[32] Omato A et al. Volatile components of plumeria flowers. Part I and Part II. Flavour Fragr J 1991;6:277-279 and 1992;7:33-35.

[33] Kaiser R. The scent of orchids – olfactory and chemical investigations. Amsterdam: Elsevier; 1993.

[34] Baldry J, Dougan J, Howard GE. Volatile flavouring constituents of durian. Phytochemistry 1972;11:2081-2084.

[35] Borg-Karlson AK, Englund FO and Unelius CR. Dimethyl oligosulphides, major volatiles released from Sauromatum guttatum and Phallus impudicus. Phytochemistry 1994;35(2):321-323.

[36] Baldwin EA. Fruit and Vegetable Flavor (Raspberry). USDA/ARS, Citrus and Subtropical Products Laboratory, Winter Haven, FL, USA, 2003.

[37] Schultz K, Kraft P. J Essent Oil Res 1997;9:509-514.

[38] Hasegawa Y et al. Characteristic components found in the essential oil of Ocimum basilicum. Flavour Fragr J 1997;12:195-200.

[39] Fernandez X et al. Volatile constituents of benzoin gums: Siam and Sumatra. Part 1. Flavour Fragr J 2003;18:328-333.

[40] Demirci B, Can Baser KH. Essential oils from the buds of Betula spp. growing in Turkey. Flavour Fragr J 2003;18:87-90.

[41] Vuorinen, T. et al. (University of Kuopio, Department of Ecology and Environmental Science, Finland)
Abs # 307: Silver birch clones are capable of emitting high amounts of terpenes under stress. American Society of Plant Biologists, Plant Biology 2003, Friday, July 25 - Wednesday July 30, 2003 - Honolulu, Hawaii USA.

[42] Leffingwell Reports, Vol. 2 (No. 4), October, 2002. www.leffingwell.com

[43] Kraft P, Bajgrowicz JA, Denis C, Fráter G. Odds and trends: Recent developments in the chemistry of odorants. Angew Chem Int Ed 2000;39:2980-3010.

[44] Kraft P, Eichenberger W. Conception, characterization and correlation of new marine odorants. Eur J Org Chem 2003:3735-3743.

[45] Chemat S et al. Comparison of conventional and ultrasound-assisted extraction of carvone and limonene from caraway seeds. Flavour Fragr J 2004;19:188-195.

[46] Jayaprakasha GK et al. Chemical composition of the flower oil of Cinnamomum zeylanicum. J Agric Food Chem 2000;48(9):4294-4295.

[47] Bianchini A et al. Composition of Helichrysum italicum essential oil from Corsica (France). Flavour Fragr J 2001;16:30-34.

[48] Bianchini A et al. A comparative study of volatile constituents of two Helichrysum italicum subspecies growing in Corsica (France), Tuscany and Sardinia (Italy). Flavour Fragr J 2003;18:487-491.

[49] Yukawa C et al. Mono- and sesquiterpenoids of the volatile oil of Bursera graveolens. Flavour Fragr J 2005;20:653-658.

[50] Yukawa C et al. Terpenoids of the volatile oil of Bursera graveolens. Flavour Fragr J 2004;19:565-570.

[51] Jirovetz L, Buchbauer G, Ngassoum MB. Solid-phase-microextraction-headspace aroma compounds of coconut (Cocos nucifera) milk and meat from Cameroon. Ernährung/Nutrition 2003;27(7/8):300-303.

[52] Emura M et al. The volatile constituents of the coffee flower (Coffea arabica). Flavour Fragr J 1997;12:9-13.

[53] Deng C et al. Determination of the volatile constituents of Chinese Coriandrum sativum by gas chromatography - mass spectrometry with solid-phase microextraction. Chromatographia 2003;57(5/6):357.

[54] Eyres G et al. Identification of character-impact odorants in coriander and wild coriander leaves using GC-olfactometry and GC x GC-TOFMS. 11th Weurmann Flavour Research Symposium, 21-24 June, 2005, Roskilde, Denmark.

[55] Bauer K, Garbe D. Common fragrance and flavor materials: preparation, properties and uses. Weinheim: VCH; 1985.

[56] Boehlens MH, van Gemert L. Physicochemical parameters related to organoleptic properties of flavour components. Perfum Flavor 1987;12(5):31-43.

[57] Näf R, Velluz A. Sulphur compounds and some uncommon esters in durian (Durio zibethinus). Flavour Fragr J 1996;11(5):295-303.

[58] Weenen H, Koolhaas WE, Apriyantono A. Sulfur-containing volatiles of durian fruits (Durio zibethinus). J Agric Food Chem 1996;44:3291-3293.

[59] Girardon P, Sauvaire Y, Baccou JC, Bessiere JM. Identification de la 3-hydroxy-4,5-dimethyl-2(5H)-furanone dans des graines de fenugrec (Trigonella foenum-graecum L.). Lebensm Wiss Technol 1986;19:44-46.

[60] Yu TH, Wu CM, Liou YC. Volatile compounds from garlic. J Agric Food Chem 1989;37:725-730.

[61] Beilsteins Handbuch der organischen Chemie / Crossfire 2006.

[62] Weyerstahl P et al. Constituents of commercial labdanum oil. Flavour Fragr J 1998;13:295-318.

[63] Ramalho PS et al. Volatile components of Cistus ladaniferus leaves. Flavour Fragr J 1999;14:300-302.

[64] Fiorini C, Fourasté I, David B, Bessière JM. Composition of the flower, leaf and stem essential oils from Laurus nobilis. Flavour Fragr J 1997;12:91-93.

[65] Mimica-Dukic N et al. Antimicrobial and antioxidant activities of Melissa officinalis (Lamiaceae) essential oil.
J Agric Food Chem 2004;52:2485-2489.

[66] Surburg H, Güntert M. Headspace technology in perfumery: Investigations of floral fragrances. H&R Contact 1991;51:12-17. (Haarmann & Reimer, now Symrise)

[67] Kreck M, Mosandl A. Synthesis, structure elucidation, and olfactometric analysis of lilac aldehyde and lilac alcohol stereoisomers. J Agric Food Chem 2003;51:2722-2726.

[68] Chisholm MG, Wilson MA, Gaskey GM. Characterization of aroma volatiles in key lime essential
oils (Citrus aurantifolia). Flavour Fragr J 2003;18:106-115.

[69] Effmert U et al. Floral benzenoid carboxyl methyltransferases: From in vitro to in planta function. Phytochemistry 2005;66:1211–1230.

[70] The Merck Index. Eleventh edition. Rahway, N.J.: Merck & Co., Inc.; 1989.

[71] Kabanov VS, Evstratova RI. A gas-chromatographic method of determining ledol in the essential oil, leaves, and herbage of Ledum palustre. Chemistry of Natural Compounds 1978;14(6):608 - 611.

[72] Brunke EJ, Hammerschmidt FJ, Schmaus G. Flower scent of some traditional medicinal plants. In: Teranishi R, Buttery RG, Sugisawa H, editors. Bioactive volatile compounds from plants. Washington: ACS Symposium Series No. 525, Amer. Chem. Soc. 1993; 282-296.

[73] The combined chemical dictionary. Web version. Chapman & Hall / CRC Press 2004.

[74] Hamm S, Bleton J, Connan J, Tchapla A. A chemical investigation by headspace SPME and GC-MS of volatile and semi-volatile terpenes in various olibanum samples. Phytochemistry 2005;66:1499-1514.

[75] Castel C et al. Volatile constituents of benzoin gums: Siam and Sumatra, part 2. Study of headspace sampling methods. Flavour Fragr J 2006;21:59-67.

[76] Novak J et al. Determination of growing location of marjoram (Origanum majorana) samples by comparison of essential oil profiles. Flavour Fragr J 2004;19:263-267.

[77] Baranska M et al. Chemotaxonomy of aromatic plants of the genus Origanum via vibrational spectroskopy. Anal Bioanal Chem 2005;381:1241-1247.

[78] Givaudan Media Release, Geneva 9 December 2003.

[79] Raina VK et al. Essential oil composition of 'kewda' (Pandanus odoratissimus) from India. Flavour Fragr J 2004;19:434-436.

[80] Aubert C, Baumann S, Arguel H. Optimization of the analysis of flavor volatile compounds by liquid-liquid microextraction (LLME). Application to the aroma analysis of melons, peaches, grapes, strawberries, and
tomatoes. J Agric Food Chem 2005;53:8881-8895.

[81] Bernhard RA, Shibamoto T, Yamaguchi K, White E. The volatile constituents of Schinus molle. J Agric Food Chem 1983;31(2):463-466.

[82] Gopalan B, Goto M, Kodama A, Hirose T. Supercritical carbon dioxide extraction of turmeric (Curcuma longa).
J Agric Food Chem 2000;48:2189-2192.

[83] Latrasse A, Rigaud J, Sarris J. L’arome du cassis (Ribes nigrum): Odeur principale et notes secondaires. Sci Aliments 1982;2:145-162.

[84] Le Quere JL, Latrasse A. Composition of the essential oils of blackcurrant buds (Ribes nigrum). J Agric Food Chem 1990;38:3-10.

[85] Smith et al. Holzforschung 1989;43:293-296.

[86] Omidbaigi R, Sefidkon F, Kazemi F. Influence of drying methods on the essential oil content and composition of Roman chamomile. Flavour Fragr J 2004;19:196–198.

[87] Knapp H et al. (S)-3,7-Dimethyl-5-octene-1,7-diol and related oxygenated monoterpenoids from petals of Rosa damascena. J Agric Food Chem 1998;46:1966-1970.

[88] Jirovetz L et al. Solid phase microextraction/gas chromatographic and olfactory analysis of the scent and fixative properties of the essential oil of Rosa damascena from China. Flavour Fragr J 2005;20:7–12.

[89] Joichi A et al. Volatile components of tea-scented modern roses and ancient Chinese roses. Flavour Fragr J 2005;20:152–157.

[90] Ravid U et al. Identification of (1R)(+)-Verbenone in Essential Oils of Rosmarinus officinalis L. Flavour Fragr J 1997;12:109-112.

[91] Pintore G et al. Chemical composition and antimicrobial activity of Rosmarinus officinalis L. oils from Sardinia and Corsica. Flavour Fragr J 2002;17:15–19.

[92] Angioni A et al. Chemical Composition, Plant Genetic Differences, Antimicrobial and Antifungal Activity Investigation of the Essential Oil of Rosmarinus officinalis L. J Agric Food Chem 2004;52:3530-3535.

[93] De Feo V, De Simone F, Senatore F. Potential allelochemicals from the essential oil of Ruta graveolens. Phytochemistry 2002;61:573–578.

[94] Cadwallader KR, Baek HH, Cai M. Spices - flavor chemistry and antioxidant properties. In: Risch SJ, Ho CT, editors. ACS Symp. Ser. 660. Washington DC, American Chemical Society, 1997. pp. 66–79.

[95] Winterhalter P, Straubinger M. Saffron - renewed interest in an
ancient spice. Food Rev Int 2000;16(1):39-59.

[96] D’Auria M, Mauriello G, Rana GL. Volatile organic compounds from saffron. Flavour Fragr J 2004;19:17–23.

[97] Benyoussef E-H, Yahiaoui N, Khelfaoui A, Aid F. Water distillation kinetic study of spearmint essential oil and of its major components. Flavour Fragr J 2005;20:30–33.

[98] Ishihara M et al. New pyridine derivatives and basic components in spearmint oil
(Mentha gentilis f. cardiaca) and peppermint oil (Mentha piperita). J Agric Food Chem 1992; 40:1647-1655.

[99] Lederer I, Schulzki G, Gross J, Steffen J-P. Combination of TLC and HPLC-MS/MS methods. Approach to a rational quality control of Chinese star anise. J Agric Food Chem 2006;54:1970-1974.

[100] Ménager I, Jost M, Aubert C. Changes in physicochemical characteristics and volatile
constituents of strawberry (Cv. Cigaline) during maturation. J Agric Food Chem 2004;52:1248-1254.

[101] De Boishebert V, Urruty L, Giraudel J-L, Montury M. Assessment of strawberry aroma through solid-phase microextraction-gas chromatography and artificial neuron network methods. Variety classification versus growing years. J Agric Food Chem 2004;52:2472-2478.

[102] Edwards KG, Stoker JR. Biosynthesis of coumarin: the isomerization stage. Phytochemistry 1967;6:655-661.

[103] Omidbaigi R, Sefidkon F, Hejazi M. Essential oil composition of Thymus x citriodorus L. cultivated in Iran. Flavour Fragr J 2005;20:237–238.

[104] Leffingwell Reports, Vol. 2 (No. 6), October, 2002. www.leffingwell.com

[105] Maurer B, Hauser A. Identification and synthesis of new gamma-lactones from tuberose absolute (Polianthes tuberosa). Helvetica Chimica Acta 1982;65(2):462-476.

[106] Kaiser R, Lamparsky D. Das Lacton der 5-hydroxy-cis-2,cis-7-Decadiensaeure und weitere Lactone aus dem Absolue der Blueten von Polianthes tuberosa. Tetrahedron Letters 1976;20:1659-1660.

[107] Bos R et al. Composition of the essential oils from underground parts of Valeriana officinalis L. and several closely related taxa. Flavour Fragr J 1997;12:359-370.

[108] Torsell K, Wahlberg K. The structure of the principal alkaloid from Valeriana officinalis. Tetrahedron Letters 1966;4:445-448.

[109] Bellesia F et al. Biosynthesis of nepetalactone in Nepeta cataria. Phytochemistry 1984;23(1):83-87.

[110] Pérez-Silva A et al. GC–MS and GC–olfactometry analysis of aroma compounds in a representative organic aroma extract from cured vanilla (Vanilla planifolia G. Jackson) beans. Food Chemistry 2006, in press.

[111] Schulte-Elte KH, Ohloff G et al. Vitispiranes, important constituents of vanilla aroma. Helvetica Chimica Acta 1978;61(106):1125-1133.

[112] Gaydou EM, Randriamiharisoa R, Bianchini JP. Composition of the essential oil of ylang-ylang (Cananga odorata Hook Fil. et Thomson forma genuina) from Madagascar. J Agric Food Chem 1986;34:481-487.

[113] Towers GHN, Tse A, Maass WSG. Phenolic acids and phenolic glycosides of Gaultheria species. Phytochemistry 1966;5:677-681.

[114] Jap. Pat. Appln. 63 083 018 (priority JA 29 Sept. 1986).

[115] Segal R, Breuer A, Feuerstein I. Irregular monoterpene alcohols from Artemisia herba-alba. Phytochemistry 1980;19:2761-2762.

[116] Khafagy SM, Gharbo SA, Sarg TM. Planta Med 1971;20:90.

[117] Abe S. J Chem Soc Jpn 1937;58:246.

[118] Topul Rali, Ph.D., University of Papua New Guinea, School of Natural & Physical Sciences, P.O. Box 24, University NCD, Papua New Guinea, Phone +675-3267222, e-mail: rali.topul@upng.ac.pg.

[119] Harms D, Nietzsche F, Hoffmann A, David F, Sandra P. The analysis of the bitter and other flavour compounds in beer and worth by stir bar sorptive extraction (SBSE) followed by HPLC. Gerstel AppNote 5/2001.

[120] Keukeleire JD et al. Formation and accumulation of alpha-acids, beta-acids, desmethylxanthohumol, and xanthohumol during flowering of hops (Humulus lupulus L.). J Agric Food Chem 2003;51:4436-4441.

[121] Eri S, Khoo BK, Lech J, Hartman TG. Direct thermal desorption-gas chromatography and gas chromatography-mass spectrometry profiling of hop (Humulus lupulus L.) essential oils in support of varietal characterization. J Agric Food Chem 2000;48:1140-1149.

[122] Steinhaus M, Schieberle P. Comparison of the most odor-active compounds in fresh and dried hop cones (Humulus lupulus L. Variety Spalter Select) based on GC-olfactometry and odor dilution techniques. J Agric Food Chem 2000;48:1776-1783.

[123] Pini GF et al. A headspace solid phase microextraction (HS-SPME) method for the chromatographic determination of alkylpyrazines in cocoa samples. J Braz Chem Soc 2004;15(2):267-271.

[124] Krings U et al. Thin-layer high-vacuum distillation to isolate volatile flavour compounds of cocoa powder. Eur Food Res Technol 2006 (in press).

[125] Counet C et al. Use of gas chromatography-olfactometry to identify key odorant compounds in dark chocolate. Comparison of samples before and after conching. J Agric Food Chem 2002;50:2385-2391.

[126] Pickenhagen W, P Dietrich. Identification of the bitter principles of cocoa. Helvetica Chimica Acta 1975;58(115):1078-1086.

[127] Smit HJ, Gaffan EA, Rogers PJ. Methylxanthines are the psycho-pharmacologically active constituents of chocolate. Psychopharmacology 2004;176:412-419.

[128] Counet C, Callemien D, Collin S. Chocolate and cocoa: New sources of trans-resveratrol and trans-piceid. Food Chemistry 2006;98:649-657.

[129] Buttery RG, Flath RA, Mon TR, Ling LC. Identification of germacrene D in walnut and fig leaf volatiles. J Agric Food Chem 1986;34:820-822.

[130] Dobson HEM et al. Pollen and flower volatiles in two Rosa species. Phytochemistry 1987;26(12):3171-3173.

[131] Hashidoko Y. The phytochemistry of Rosa rugosa. Phytochemistry 1996;43(3):535-549.

[132] Brodnitz MH, Pascale JV. Thiopropanal S-oxide: A lachrymatory factor in onions. J Agric Food Chem 1971;19(2):269-272.

[133] Block E et al. Allium chemistry: synthesis of 1-[alk(en)ylsulfinyl]propyl alk(en)yl disulfides (cepaenes), antithrombotic flavorants from homogenates of onion (Allium cepa). J Agric Food Chem 1997;45:4414-4422.

[134] Randle WM et al. Onion (Allium cepa L.) thiosulfinates respond to increasing sulfur fertility. J Agric Food Chem 1994;42:2085-2088.

[135] Schmidt NE et al. Rapid extraction method of quantitating the lachrymatory factor of onion using gas chromatography. J Agric Food Chem 1996;44:2690-2693.

[136] Rout PK, Naik SN, Rao YR. Composition of the concrete, absolute, headspace and essential oil of the flowers of Michelia champaca L. Flavour Fragr J 2006;21:906-911.

[137] Kaiser R. New natural products of structural and olfactory interest identified in fig leaf absolute (Ficus carica). In: Progress in Essential Oil Research. Berlin, New York: Walter de Gruyter & Co.; 1986.

[138] Crews C et al. Study of the main constituents of some authentic walnut oils. J Agric Food Chem 2005;53:4853-4860.

[139] Stampar F et al. Traditional walnut liqueur - cocktail of phenolics. Food Chemistry 2006;95:627-631.

[140] Fukuda T, Ito H, Yoshida T. Antioxidative polyphenols from walnuts (Juglans regia L.). Phytochemistry 2003;63:795-801.

[141] Elmore JS, Nisyrios I, Mottram DS. Analysis of the headspace aroma compounds of walnuts (Juglans regia L.). Flavour Fragr J 2005;20:501-506.

[142] Tajima et al. Analysis of green and yellow yuzu peel oils (Citrus junos Tanaka). Novel aldehyde components with remarkably low odour thresholds. J Agric Food Chem 1990;38:1544-1548.

[143] Matsuura Y, Hata G, Abe S, Sakai I, Abe A. Tech. Data of the 8'th International Congress of Essential Oils. Cannes, France; 1980;497-499.

[144] Rodefeld L, Tochtermann W. A new approach to (9Z)-dodec-9-en-12-olide (yuzu lactone) via phase transfer catalysis cyclization. Tetrahedron 1998;54:5893-5898.

[145] Song HS et al. Quantitative determination and characteristic flavour of Citrus junos (yuzu) peel oil. Flavour Fragr J 2000;15:245-250.

[146] Surburg H, Panten J. Common fragrance and flavor materials. Preparation, properties and uses. 5th completely revised and enlarged edition. Weinheim: Wiley-VCH; 2006.

[147] Appendino G et al. Coumarins from Opopanax chironium. New Dihydrofuranocoumarins and differential induction of apoptosis by imperatorin and heraclenin. J Nat Prod 2004;67:532-536.

[148] Beaulieu JC, Lea JM. Characterization and semiquantitative analysis of volatiles in
seedless watermelon varieties using solid-phase microextraction. J Agric Food Chem 2006;54:7789-7793.

[149] Scheffer JJC, Baerheim Svendsen A. Internationaal symposium: Voorkomen en analyse van etherische oliën, Marburg, 8-9 juni 1981. Pharmacy World & Science 1981;3(1):1417-1419.

[150] Mediavilla V, Steinemann S. Essential oil of Cannabis sativa L. strains. Journal of the International Hemp Association 1997;4(2):82.

[151] Novak J et al. Essential oils of different cultivars of Cannabis sativa L. and their antimicrobial activity. Flavour Fragr J 2001;16:259-262.

[152] Alasalvar C et al. Comparison of natural and roasted Turkish Tombul hazelnut (Corylus avellana L.) volatiles and flavor by DHA/GC/MS and descriptive sensory analysis. J Agric Food Chem 2003;51:5067-5072.

[153] Blanch GP, Jauch J. Enantiomeric composition of filbertone in hazelnuts in relation to extraction conditions. Multidimensional gas chromatography and gas chromatography/mass spectrometry in the single ion monitoring mode of a natural sample. J Agric Food Chem 1998;46:4283-4286.

[154] Schroll W, Nitz S and Drawert F. Vorkommen von resorcindimethylether in rohen haselnussen. Chem Mikrobiol Technol Lebensm 1987;10:188.

[155] Rogerson FSS et al. 1,3-Dimethoxybenzene, a newly identified component of port wine. J Sci Food Agric 82:1287-1292 (online 2002).

[156] Nerali SB, Kalsi PS. Terpenoids LXXVII. Structure of isopatchpulenone, a new sesquiterpene ketone from the oil of Cyperus scariosus. Tetrahedron Letters 1965;45:4053-4056.

[157] Satinder KU, Chhabra BR, Kalsi PS. A biogenetically important hydrocarbon from Cyperus scariosus. Phytochemistry 1984;23(10):2367-2369.

[158] Buttery RG, Kamm JA, Ling LC. Volatile components of red clover leaves, flowers, and seed pods: possible insect attractants. J Agric Food Chem 1984;32:254-256

[159] Rali T, Wossa SW, Leach DN. Comparative chemical analysis of the essential oil constituents in the bark, heartwood and fruits of Cryptocarya massoy (Lauraceae) from Papua New Guinea. Molecules 2007;12:149-154.

[160] Jiang L, Kubota K. Differences in the volatile components and their odor characteristics of green and ripe fruits and dried pericarp of Japanese pepper (Xanthoxylum piperitum DC.). J Agric Food Chem 2004;52:4197-4203.

[161] Sugai E, Morimitsu Y, Kubota K. Quantitative analysis of sanshool compounds in Japanese pepper (Xanthoxylum piperitum DC.) and their pungent characteristics. Biosci Biotechnol Biochem 2005;69(10):1958-1962.

[162] Macleod AJ, Islam R. Volatile flavour components of watercress. J Science Food Agric 1975;10:1545-1550.

[163] Murray KE, Whitfield FB. The occurrence of 3-alkyl-2-methoxypyrazines in raw vegetables. J Science Food Agric 1975;26(7):973-986.

[164] Maarse H, editor. Volatile Compounds in Foods and Beverages. New York: Dekker; 1991, p. 234.

[165] Waring RH, Mitchell SC, Fenwick GR. The chemical nature of the urinary odour produced by man after asparagus ingestion. Xenobiotica 1987;17:1363-1371.

[166] Mitchell SC. Food idiosyncrasies: beetroot and asparagus. Drug Metabolism and Disposition 2001;29(4):539-543.

[167] Kaiser R. Meaningful scents around the world. Olfactory, chemical, biological, and cultural considerations. Zürich: Verlag Helvetica Chimica Acta, Wiley-VCH; 2006.

[168] Kessler D, Baldwin I. Making sense of nectar scents: the effects of nectar secondary metabolites on floral visitors of Nicotiana attenuata. The Plant Journal 2006;49:840–854.

[169] Danute Pajaujis Anonis. The application of carnation in perfumery. Flavour Fragr J 1985;1: 9-15.

[170] Burnett A R, Thomson R H. J. Chem. Soc. C. 1968:854-857.

[171] Berenbaum M. Coumarins and caterpillars: A case for coevolution. Evolution 1983;37(1):163-179.

[172] Wörner M, Schreier P. Über die Aromastoff-Zusammensetzung von Waldmeister (Galium odoratum). Zeitschrift für Lebensmitteluntersuchung und -Forschung. 1991;193:317-320.

[173] Pino JA, Mesa J. Contribution of volatile compounds to mango (Mangifera indica) aroma. Flavour Fragr J 2006;21(2):207-213.

[174] Pino JA, Mesa J, Muños Y, Marti MP, Marbot R. Volatile components from Mango (Mangifera indica) cultivars. J Agric Food Chem 2005;53(6):2213-2223.

[175] Kollmannsberger H, Lorenz M, Weinreich B, Nitz S. The flavour composition of Manzanilla de la Montaña (Helenium aromaticum) from Chile. Advances in food sciences 1998;20(3-4):122-131.

[176] Berger RG, Drawert F, Kollmannsberger H. The flavour of cape gooseberry (Physalis peruviana). Zeitschrift für Lebensmitteluntersuchung und -Forschung 1989;188(2)122-126.

[177] Carbonell-Barrachina AA, Agusti A, Ruiz JJ. Analysis of flavor volatile compounds by dynamic headspace in traditional and hybrid cultivars of Spanish tomatoes. European Food Research and Technology 2006;222(5-6):536-542.

[178] Jirovetz L, Smith D, Buchbauer G. Aroma compound analysis of Eruca sativa (Brassicaceae) SPME headspace leaf samples using GC, GC-MS, and olfactometry. J Agric Food Chem 2002;50(16):4643-4646.

[179] Miyazawa M, Maehara T, Kurose K. Composition of the essential oil from the leaves of Eruca sativa. Flavour Fragr J 2002;17(3):187-190.

[180] Maia et al. Essential oils of Toona and Cedrela Species (Meliaceae): Taxonomic and ecological implications. J Braz Chem Soc 2000;11(6):629-639.

[181] Asekun OT, Ekundayo O. Constituents of the leaf essential oil of Cedrela odorata from Nigeria. Flavour Frag J 1999;14(6)390-392.

[182] Møhl B et al. (2000). Sperm whale clicks: Directionality and source level revisited. J Acoustic Soc Am 2000;107(1):638-648.

[183] Madsen P et al. Sperm whale sound production studied with ultrasound time-depth-recording tags. J Exp Biol 2002;205:1899-1906.

[184] Duke JA. Handbook of legumes of world economic importance. New York: Plenum Press; 1981.

[185] Demole E, Enggist P, Stoll M. Sur les constituants odorants de l'essence absolue de Cassie (Acacia farnesiana). Helvetica Chimica Acta 1969;52(1):24-32.

[186] Benkaci-Ali F et al. Chemical composition of seed essential oils from Algerian Nigella sativa extracted by microwave and hydrodistillation. Flavour Fragr J 2006;22(2):148-153.

[187] Pommerehne H. Ueber das Damascenin, ein Bestandteil der Samen von Nigella damascena L. Archiv der Pharmazie 2006;237(6):475-480.

[188] Lu G, Edwards CG, Fellman JK, Mattinson DS, Navazio J. Biosynthetic origin of geosmin in red beets (Beta vulgaris L.). J Agric Food Chem 2003;51(4):1026-9.

[189] van Dort et al. Narcissus trevithian and Narcissus geranium: Analysis and synthesis of compounds. J Agric Food Chem 1993;41:2063-2075.

[190] Kaiser R. Environmental scents at the Ligurian coast. Perfumer & Flavorist 1977;7:7-18.

[191] Sell CS. A fragrant introduction to terpenoid chemistry. Cambridge: RSC; 2003.

[192] Kamden PD, Hanover JW, Gage DA. Contribution to the study of the essential oil of Thuja occidentalis L. J Essent Oil Res 1993;5(2):117-122.

[193] Ho TL. A total synthesis of dl-occidol. Canadian Journal of Chemistry 1972;50:1098-1099.

[194] Mane RB, Kadam AJ. A new synthesis of occidol. Collect Czech Chem Commun 1999;64:533-538.

[195] Rout PK, Naik SN, Rao YR. Subcritical CO2 extraction of floral fragrance from Quisqualis indica L. The Journal of Supercritical Fluids 2008;45(2):200-205.

[196] Eisikowitch D, Rotem R. Flower orientation and color change in Quisqualis indica and their possible role in pollinator partitioning. Botanical Gazette 1987;148(2):175-179.

[197] Okamoto T et al. J Biol Chem, 1998;273(21);13089-13096.

[198] Tohar N et al. A comparative study of the essential oils of the genus Plumeria L. from Malaysia. Flavour Fragr J 2006;21(6):859-863.

[199] Thiamacrolides. EP19980102035 (Frater G. Kraft P. Bajgrowicz J. Givaudan Roure Int. 1998).

[200] Hatanaka A. The biogeneration of green odour by green leaves. Phytochemistry 1993;34:1201-1218.

[201] Hatanaka A, Kujiwara T, Matsui K. The biogeneration of green odour by green leaves and its physiological functions - past, present and future. Z Naturforsch 1995;50:467-472.

[202] Ueyama Y, Arai T, Hashimoto S. Volatile constituents of ethanol extracts of Hierochloe odorata L. var. pubescens kryl. Flavour Fragr J 1991;6(1):63-68.

[203] Yamamoto Y. Allelopathic potential of Anthoxanthum odoratum for invading Zoysia-grassland in Japan. Journal of Chemical Ecology 1995;21(9):1365-1373.

[204] Perkin WH. Berichte 1875;8:1599.

[205] Paine S. In a chocolate garden. New Scientist 2008;200(2684): 48-49.

[206] Da Costa NC, Pantini M. The analysis of volatiles in Tahitian vanilla (Vanilla tahitensis) including novel compounds. In: Bredie WLP, Petersen MA, editors. Developments in food science, Flavour science - recent advances and trends 2006;43: 161-164.

[207] Joulain D, Tabacchi R. Two volatile beta-chromenes from Wisteria sinensis flowers. Phytochemistry 1994;37:1769-1770.

[208] Garnero J, Joulain D. In: Proceedings of the 9th International Congress of Essential Oils, Singapore 13-17 March 1983: 184-193.

[209] Torrado et al. Volatile constituents from tamarillo (Cyphomandra betacea Sendtn.) fruit. Flavour Fragr J 1995;10(6):349-354.

[210] Brunke EJ, Ritter F, Schmaus G. New data on trace components with sensory relevance in flower scents. Dragoco Report 1996;1:5-21.

[211] Nishimura, O, Masuda H, Mihara S. Hydroxy nitriles in blackcurrant buds absolute (Ribes nigrum L.). J Agric Food Chem 1987;35(3):338-340.

[212] Chisholm MG, Jell JA, Cass Jr DM. Characterization of the major odorants found in the peel oil of Citrus reticulata Blanco cv. Clementine using gas chromatography-olfactometry. Flavour Fragr J 2003;18(4):275-281.

[213] Puxbaum H, König G. Observation of dipropenyldisulfide and other organic sulfur compounds in the atmosphere of a beech forest with Allium ursinum ground cover. Short communication. Atmospheric Environment 1997;31(2):291-294.

[214] Joulain D. The composition of the headspace from fragrant flowers: Further results. Flavour Fragr J 1987;2:149-155.

[215] Lopes D, Kolodziejczyk P. Essential Oil Composition of Pineapple-weed (Matricaria discoidea DC.) grown in Canada. Journal of Essential Oil Bearing Plants 2005;8(2):178-182.

[216] Ma CM, Winsor L, Daneshtalab M. Quantification of spiroether isomers and herniarin of diffrent parts of Matricaria matricarioides and flowers of Chamemelum nobile. Phytochem Anal 2007;18(1):42-9.

[217] Hänsel R, Keller K, Rimpler H, Schneider G, editors. Hagers Handbuch der Pharmazeutischen Praxis, 5 Drogen E-O. Berlin, Heidelberg: Springer Verlag; 1993.

[218] Naves YR. Présence de maaliol et de valéranone dans l'huile essentielle de Spikenard (Nardostachys jatamansi) chinoise. Helvetica Chimica Acta 1963;46:2139-2141.

[219] Venkateswara RG, Annamalai T, Mukhopadhyay T. Nardal, a new sesquiterpene aldehyde from the plant Nardostachys jatamansi. Indian Journal of Chemistry. Sect. B. 2008;47(1):163-165.

[220] Burfield T. Updated list of threatened aromatic plants used in the aroma & cosmetic industries v. 1.10, 2009. www.cropwatch.org

[221] Wright CW, editor. Artemisia. London: Taylor & Francis; 2002.

[222] Thomas AF, Pitton G. The isolation, structure, and synthesis of davana ether, an odoriferous compound of the oil of Artemisia pallens. Helv Chim Acta 1971;54(7):1890-1891.

[223] Mallavarapu GR, Kulkarni RN, Baskaran K, Rao L, Ramesh S. Influence of plant growth stage on the essential oil content and composition in Davana (Artemisia pallens). J Agric Food Chem 1999;47(1):254-258.

[224] Pino JA, Cuevas-Glory L, Fuentes V. Volatile Components of Mabolo (Diospyros blancoi) grown in Cuba.
J Essent Oil Res
2008;20(6):506-508.

[225] Collins RP, Halim AF. Characterization of the volatile compounds of Diospyros blancoi.
Economic Botany
1976;30(4):313-316.

[226] Burfield T. Cropwatch No. 6, October 2004.

[227] Chantraine JM, Dhénin JM, Moretti C. Chemical variability of rosewood (Aniba rosaerodora) essential oil in French Guiana. J Essent Oil Res 2009;21(6):486-495.

[228] Vilegas JH, Lancas FM, Vilegas W. Composition of the volatile compounds from Aniba canelilla extracted by CO2 in the supercritical state. Rev Bras Farmacogn 1998;7-8(1):13-19.

[229] Lahlou S et al. Cardiovascular effects of the essential oil of Aniba canelilla bark in normotensive rats. Journal of Cardiovascular Pharmacology 2005;46(4):412-421.

[230] Kasali AA, Oyedeji AO, Ashilokun AO. Volatile leaf oil constituents of Cymbopogon citratus. Flavour Fragr J 2001;16(5):377-378.

[231] Vietmeyer ND, editor. Vetiver grass: A thin green line against erosion. Board on Science and Technology for International Development. National Research Council. Washington, D.C.: National Academy Press; 1993.

[232] Weyerstahl P, Marschall H, Splittgerber U, Wolf D, Surburg H. Constituents of Haitian vetiver oil. Flavour Fragr J 2000;15(6):395-412.

[233] Champagnat P et al. A study on the composition of commercial Vetiveria zizanioides oils from different geographical origins. J Essent Oil Res 2006;18(4):416-422.

[234] Ling L, Guoxin S, Yaoming H. GC-MS analysis of the essential oil from Piper nigrum and Piper longum. Chromatographica 2007;66(9-10):785-790.

[235] Clery RA, Hammond CJ, Wright AC. Nitrogen-containing compounds in black pepper oil (Piper nigrum).
J Essent Oil Res 2006;18(1):1-3.

[236] Jirovetz L, Buchbauer G, Ngassoum MB, Geissler M. Aroma compound analysis of Piper nigrum and Piper guineense essential oils from Cameroon using solid-phase microextraction-gas chromatography, solid-phase microextraction-gas chromatography-mass spectrometry and olfactometry. J Chromatography A 2002;976(1-2):265-275.

[237] Gaikar et al. US Patent No. 6,365,601 B1, Apr. 2, 2002.

[238] Jansz ER, Pathirana IC, Packiyasothy EV. Determination of piperine in pepper (Piper nigrum). J Natn Sci Coun Sri Lanka 1983;11(1):129-138.

[239] Myers RL. The 100 most important chemical compounds: A reference guide. Westport, CT: Greenwood Press; 2007.

[240] Steinhaus M, Schieberle P. Role of the fermentation process in off-odorant formation in white pebber: On-site trial in Thailand. J Agric Food Chem 2005;53:6056-6060.

[241] Möller H. Phototoxicity of Dictamnus albus. Contact Dermatitis 1978;4:264-269.

[242] Baser KHC, Kosar M, Malyer H, Ozek T. The essential oil composition of Dictamnus albus from Turkey. Planta Medica 1994;60:481-2.

[243] Fleisher A, Fleisher Z. Study of Dictamnus gymnostylis (D. albus) volatiles and plausible explanation of the "burning bush" phenomenon. J Essent Oil Res 2004;16(1),1–3.

[244] Liu YL, Deng ZF. Investigation of the chemical constituents of the essential oil of Houttuynia cordata. Acta Botanica Sinica 1979;21:244-249.

[245] Tutupali LV, Chaubal MG. Saururaceae. V. Composition of essential oil from foliage of Houttuynia cordata and chemosystematics of Saururaceae. Journal of Natural Products 1975;38:92-96.

[246] Pröbstle A et al. Novel pyridine and 1,4-dihydropyridine alkaloids from Houttuynia cordata. Natural Product Research 1994;4(3):235-240.

[247] Surburg H, Guentert M, Harder H. Volatile compounds from flowers: Analytical and olfactory aspects. In: Teranishi R, Buttery RG, Sugisawa H, editors. Bioactive volatile compounds from plants. ACS Symposium Series 525. Washington, DC: American Chemical Society; 1993.

[248] CITES (Convention on International Trade in Endangered Species of wild fauna and flora). Fifteenth meeting of the Conference of the Parties, Doha (Qatar), 13-25 March 2010. (Proposal 42, Inclusion of Bulnesia sarmientoi)

[249] Stashenko EE, Molina JL, Mora AL, Martínez JR. In vivo HS-SPME and GC-MS analysis of volatiles from Brugmansia suaveolens flowers. The 8th Conference of the Israel Analytical Chemistry Society, January 11-12, 2005, Tel Aviv.

[250] Anthony SJ, Zuchowski W, Setzer WN. Composition of the floral essential oil of Brugmansia suaveolens. Rec Nat Prod 2009;3(2):76-81.

[251] Zayed R, Wink M. Induction of tropane alkaloid formation in transformed root cultures of Brugmansia suaveolens (Solanaceae). Z Naturforsch 2004;59c:863-867.

[252] Clark DG et al. Benzenoids dominate the fragrance of Petunia flowers. In: Gerats T, Strommer J, editors. Petunia: Evolutionary, developmental and physiological genetics. New York: Springer; 2009.

[253] Verdonk JC et al. Regulation of floral scent production in petunia revealed by targeted metabolomics. Phytochemistry 2003;62(6):997-1008.

[254] Negre F et al. Regulation of methylbenzoate emission after pollination in snapdragon and petunia flowers. The Plant Cell 2003;15:2992-3006.

[255] Nakamura K et al. Identification of Petunia hybrida cultivars that diurnally emit floral fragrances. Scientia Horticulturae 2006;108(1):61-65.

[256] Plepys D et al. Odour-mediated nectar foraging in the silver y moth, Autographa
gamma
(Lepidoptera: Noctuidae): behavioural and electrophysiological responses to floral volatiles. Oikos 2002;99:75-82.

[257] Motl O. Collect Czech Chem Commun 1973;38:3737. Referenced in: Tirillini B et al. Chemical composition and fungicidal activity of the essential oil of Laserpitium garganicum from Italy. Chemistry of Natural Compounds 2009;45(1):102-105.

[258] Rangel-Castro JI, Staffas A, Danell E. The ergocalciferol content of dried pigmented and albino Cantharellus cibarius fruit bodies. Mycological Research 2002;106(1):70-73.

[259] Pyysalo H. Identification of volatile compounds in seven edible fresh mushrooms. Acta Chemica Scandinavica 1976;30:235-244.

[260] Fons F, Rapior S. Les substances volatiles dans les genres Cantharellus, Craterellus et Hydnum. Cryptogamie, Mycologie 2003:24(4):367-376.

[261] Danell E, Camacho FJ. Successful cultivation of the golden chanterelle. Nature 1997;385(6614):303.

[262] Heck CI, González de Mejia E. Yerba mate tea (Ilex paraguariensis): A comprehensive review on chemistry, health implications, and technological considerations. Journal of Food Science 2007;72(9):138-151.

[263] Lozano PR, Cadwallader KR, González de Mejia E. Identification of characteristic aroma components of mate (Ilex paraguariensis) tea. In: Tunick MH, González de Mejia E, editors. Hispanic Foods: Chemistry and Flavor. Chapter 12, pp 143-152. ACS Symposium Series, Vol. 946. American Chemical Society; 2007.

[264] Rapior S et al. The anise-like odor of Clitocybe odora, Lentinellus cochleatus and Agaricus essettei. Mycologia 2002;94(3):373-376.

[265] Agnieszka Z et al. Comparison of volatile constituents of Acorus calamus and Asarum europaeum obtained by different techniques. The Journal of Essential Oil Research 2008;20(5):390-395.

[266] Jork H, Biering WE. Furopelargon A, ein neues Sesquiterpenketon aus dem ätherischen Öl von Asarum europaeum L. Archiv der Pharmazie 1979;312(8):681-688.

[267] Hänsel R, Keller K, Rimpler H, Schneider G, editors. Hagers Handbuch der pharmaceutischen Praxis 6: Drogen P-Z. Berlin: Springer-Verlag; 1994.

[268] Lipton RB, Göbel H, Einhäupl KM, Wilks K, Mauskop A. Petasites hybridus root (butterbur) is an effective preventive treatment for migraine. Neurology 2004;63(12): 2240–4.

[269] Fan M, Xie J, Sun B. Study on the preparation of pomelo peel oil rich in nootkatone by simultaneous distillation and solvent extraction. Food Science 2006;12.

[270] Ishida T, Suga T, Matsuura T. Conformation of nootkatone. Cellular and Molecular Life Sciences 1970;26(9):934-935.

[271] Kaiser R. 4-Hepten-2-yl salicylate and its use as fragrance ingredient. Patent No. US 7,842,660 B2; Nov. 30, 2010.

[272] Clery R. High-impact odorants in essential oils. Flavour Fragr J 2010;25(3):117-120.

[273] Joulain D. The composition of the headspace from fragrant flowers: Further results. Flavour Fragr J 1987;2:149-155.

[274] Trazzi G, André MF, Coelho F. Diastereoselective synthesis of beta-piperonyl-gamma-butyrolactones from Morita-Baylis-Hillman adducts. Highly efficient synthesis of (+/-)-Yatein, (+/-)-Podorhizol and (+/-)-epi-Podorhizol.
J Braz Chem Soc
2010;0(0):1-13.

[275] Asakawa Y. Biologically active compounds from bryophytes. Pure Appl Chem 2007;79(4):557-580.

[276] Toyota M, Asakawa Y, Frahm JT. Homomono- and sesquiterpenoids from the liverwort Lophocolea heterophylla. Phytochemistry 1990;29(7):2334-2337.

[277] Rieck A, König WA. Furano-eudesma-4(15),7,11-trien-5-alpha-ol from the liverwort Lophocolea heterophylla. Phytochemistry 1996;43(5):1055-1056.

[278] www.takasago.com

[279] Nohara I et al. Volatile constituents from the flower of Cyclamen original species (Cyclamen trochoperanthum). Koryo, Terupen oyobi Seiyu Kagaku ni kansuru Toronkai Koen Yoshishu 2000;44:29-31.

[280] Noleau I, Toulemonde B, Richard H. Volatile constituents of cardamom (Elettaria cardamomum) cultivated in Costa Rica. Flavour Fragr J 1987;2:123-127.

[281] Müller DG, Jaenicke L, Donike M, Akintobi T. Sex attractant in a brown alga: Chemical structure. Science 1971;171(3973):815-817.

[282] US Patent Application 20100130624: 4-alkyl substituted pyridines as odoriferous substances. Filed on November 20, 2009. Published on May 27, 2010 (Symrise).

[283] Anon. Essential oil of Stirlingia latifolia from Western Australia. Bull Imp Inst 1923;21:318-320.

[284] Bowen BJ, Pate JS. Effect of season burn on shoot recovery and post-fire flowering performance in the resprouter Stirlingia latifolia. Austral Ecology 2004;29(2):145-155.

[285] Takaishi K, Kawahara Y, Ikebe K. Maltol and sugars of the leaves of Cercidiphyllum japonicum. J Pharm Soc Japan 1973;93(11):1538-42.

[286] Tiefel P, Berger RG. Seasonal variation of the concentrations of maltol and maltol glucoside in leaves of Cercidiphyllum japonicum. J Sci Food and Agric 1993;63(1):59-61.

[287] Helsper JPFG et al. Identification of the volatile component(s) causing the characteristic foxy odor in various cultivars of Fritillaria imperialis L. (Liliaceae). J Agric Food Chem 2006;54(14):5087–5091.

[288] Komarek D et al. The role of 3-methyl-2-butene-1-thiol in beer flavor. In: Deibler KD, Delwiche J, editors. Handbook of flavor characterization: Sensory analysis, chemistry and physiology. CRC Press; 2003.

[289] Venton BJ, Robinson TE, Kennedy RT. Transient changes in nucleus accumbens amino acid concentrations correlate with individual responsivity to the predator fox odor 2,5-dihydro-2,4,5-trimethylthiazoline. J Neurochem 2006;96:236–246.

[290] Omori H, Nakahara K, Umano K. Characterization of aroma compounds in the peel extract of Jabara (Citrus jabara Hort. ex Tanaka). Flavour Fragr J 2011;26(6):396-402.

[291] Greger V, Schieberle P. Characterization of the key aroma compounds in apricots (Prunus armeniaca) by application of the molecular sensory science concept. J Agric Food Chem 2007;55(13):5221-5228.

[292] Guichard E. Chiral gamma-lactones, key compounds to apricot flavor: Sensory evaluation, quantification, and chirospecific analysis in different varieties. In: Fruit Flavors, ACS Symposium Series 1995;596:258-267.

[293] Schlotzhauer WS, Pair SD, Horvat RJ. Volatile constituents from the flowers of Japanese Honeysuckle (Lonicera japonica). J Agric Food Chem 1996;44(1):206-209.

[294] Ikeda N et al. Volatile components of honeysuckle (Lonicera japonica) flowers. Flavour Fragr J 1994;9(6):325-331.

[295] Wang G et al. Analysis of chemical constituents of essential oil in Lonicera japonica cultivated on the northern plain of Henan Province. Zhongguo Zhong Yao Za Zhi 1992;17(5):268-270.

[296] Fadiman J. Genista canariensis: A minor psychedelic. Economic Botany 1965;19(4):383.

[297] Zheng M et al. Analysis of volatile compounds from the flower of P. tomentosa
by SPME-GC/MS. J Chinese Mass Spect Soc 2009;2:8.

[298] Eddleston M et al. Epidemic of self-poisoning with seeds of the yellow oleander tree (Thevetia peruviana) in northern Sri Lanka. Tropical Medicine and International Health 1999;4(4):266-273.

[299] Guilherme J et al. Volatiles from the flowers of Thevetia peruviana and Allamanda cathartics (Apocynaceae).
J Esssent Oil Res 2000;12(3):322-324.

[300] Eden Botanicals. See under links!

[301] Khalid KA, Silva JAT. Biology of Calendula officinalis: Focus on pharmacology, biological activities and agronomic practices. Medicinal and Aromatic Plant Science and Biotechnology 2012;6(1):12-27.

[302] Kaskoniene V et al. Chemical composition and chemometric analysis in essential oil of Calendula officinalis during vegetation stages. Chromatographia 2012;73:163-169.

[303] Lawrence B M. Progress in essential oils. Perfumer & Flavorist 2007;32(8):44.

[304] Tateo F, Bononi M. Headspace-SPME analysis of volatiles from quince whole fruits. J Essent Oil Res 2010;22(5):416-418.

[305] Winterhalter P, Rouseff R. Carotenoid-derived aroma compounds: An introduction. In: Winterhalter P, Rouseff R, editors. Carotenoid-derived aroma compounds. ACS Symposium Series 802. Washington DC: ACS; 2001.

[306] Winterhalter P, Schreier P. 4-Hydroxy-7,8-dihydro-beta-ionol: Natural precursor of theaspiranes in quince fruit (Cydonia oblonga). J Agric Food Chem 1988;36(3):560-562.

[307] Horvat RJ, Chapman GW, Payne JA. Volatiles of ripe Flowering Quince (Chaenomeles speciosa). J Essent Oil Res 1994;6(1):81-83.

[308] Rout PK, Rao YR, Sree A, Maik SN. Composition of essential oil, concrete, absolute, wax and headspace volatiles of Murraya paniculata flowers. Flavour Fragr J 2007;22(5):352-357.

[309] Rout PK, Rao Y, Naik S. Liquid CO2 extraction of Murraya paniculata flowers. Industrial Crops and Products 2010;32(3):338-342.

[310] Naomi Okubo. Fragrance suppressor for ornamental flower. EP 2359679 A1, 2011.

[311] Kilpinen O, Liu D, Adamsen AP. Real-time measurement of volatile chemicals released by bed bugs during mating activities. Plos One 2012;7:e50981.

[312] Nickavar B, Amin G, Yosefi M. Volatile constituents of the flower and fruit oils of Pittosporum tobira grown in Iran. Z Naturforschung 2004;59c:174-176.

[313] Loukis A, Hatziioannou C. Volatile constituents of Pittosporum tobira cultivated in Greece. J Essent Oil Res 2005;17(2):186-187.

[314] Joulain D. Study of the fragrance given off by certain springtime flowers. In: Brunke EJ, editor. Progress in essential oil research. Proceedings of the International Symposium on Essential Oils, Holzminden, Germany 1985. NY: Walter de Gruyter; 1986; 57-67.

[315] Novakovic M et al. Chemical composition, antibacterial and antifungal activity of the essential oil of Cotinus coggygria from Serbia. J Serb Chem Soc 2007;72(11):1045-1051.

[316] Bakker J, Clarke RJ. Wine flavour chemistry. 2nd ed. Oxford: Wiley; 2012.

[317] Ehlers D et al. HPLC analysis of tonka bean extract. Z Lebensm Unters Forsch 1995;201:278-282.

[318] Hammami S et al. Flower essential oil composition of Tunisian Matthiola longipetala and its bioactivity against Tribolium confusum insect. Journal of Essential Oil Bearing Plants 2006;9(2):156-161.

[319] www.abp.com.au

[320] Gray PS, Mills JS. The isolation of abienol from Canada balsam, the oleoresin of Abies balsamea. J Chem Soc 1964:5822-5825.

[321] Barrero AF et al.. Synthesis of Ambrox from (-)-sclareol and (+)-cis-abienol. Tetrahedron 1993;49:10405–10412.

[322] Zerbe P et al. Bifunctional cis-abienol synthase from Abies balsamea discovered by transcriptome sequencing and its implications for diterpenoid fragrance production. J Biol Chem 2012;287(15):12121-31.

[323] Mookherjee BD, Wilson RA. Perfumer & Flavorist 1990;15(1):27-49.

[324] A method to extract borneol from the exudates of Dryobalanops aromatica. WIPO Patent Application WO 2013 / 187754.

[325] Martin D M et al. The bouquet of grapevine (Vitis vinifera L. cv. Cabernet Sauvignon) flowers arises from the biosynthesis of sesquiterpene volatiles in pollen grains. Proceedings of the National Academy of Sciences of the United States of America (PNAS) 2009;106(17):7245-7250.

[326] Buchbauer G, Jirovetz L, Wasicky M, Herlitschka A. Headspace analysis of Vitis vinifera (Vitaceae) flowers. J Essent Oil Res 1994;6:313–314.

[327] Buchbauer G, Jirovetz L, Wasicky M, Herlitschka A, Nikiforov A. Aroma of white wine flowers. Z Lebensm Unters Forsch 1994;199:1–4 (in German).

[328] Buchbauer G, Jirovetz L, Wasicky M, Nikiforov A. Aroma from red wine flowers. Z Lebensm Unters Forsch 1995;200:443–446 (in German)

[329] Aberchane M, Fechtal M, Chaouch A. Analysis of Moroccan Atlas cedarwood oil (Cedrus atlantica Manetti). J Essen Oil Res 2004;16(6):542-547.

[330] Saab AM, Harb FY, Koenig WA. Essential oil components in heart wood of Cedrus libani and Cedrus atlantica from Lebanon. Minerva Biotec 2005;17:159-62.

[331] Paoli M et al. Chemical variability of the wood essential oil of Cedrus atlantica (Manetti) from Corsica. Chem Biodivers 2011;8(2):344-51.

[332] Ferreira L, Perestrelo R, Câmara JS. Comparative analysis of the volatile fraction from Annona cherimola cultivars by solid-phase micro-extraction and gas chromatography-quadropole mass spectrometry detection. Talanta 2009;77(3):1087-1096.

[333] Lis-Balchin M. Essential oils from different Pelargonium species and cultivars: their chemical composition (using GC, GC/MS) and appearance of trichomes (under EM). In: Lis-Balchin M, editor. Geranium and Pelargonium: The genera Geranium and Pelargonium. Medicinal and Aromatic Plants - Industrial Profiles. London: Taylor & Francis; 2002.

[334] Oyama-Okubo N. Scent compounds of some scented leaf pelargonium cultivars. Bull Natl Inst Flor Sci 2010;10:55-63.

[335] Maretic M. Chemical composition of volatile compounds from Hedera helix L. honey. Graduate thesis, Faculty of Chemical Technology, University of Split, Croatia, 2011.

[336] Polatoglu K et al. Antibacterial activity and the variation of Tanacetum parthenium essential oil from Turkey. J Oleo Sci 2010;59(4):177-184

[337] Hendriks H et al. The essential oil of Tanacetum parthenium. Flavour Fragr J 1995;11(6):367-371.

[338] Banthorpe D V et al. Parthenolide and other volatiles in the flowerheads of Tanacetum parthenium. Flavour Fragr J 1990;5(3):183-185.

[339] Mathema VB. Parthenolide, a sesquiterpene lactone, expresses multiple anti-cancer and antiflammatory activities. Inflammation 2012;35(2):560-565.

[340] Pareek A et al. Feverfew (Tanacetum parthenium): A systematic review. Pharmacogn Rev 2011;5(9):103-110.

[341] Adams RP, Kauffmann M, Callahan F. The essential oil of Abies grandis: revisited 38 years later. Phytologia 2015;97(1)

[342] Scora RW et al. Contribution to the origin of the grapefruit, Citrus paradisi (Rutaceae). Systematic Botany 1982;7(2):170-177.

[343] Pattrick JG et al. A dual function for 4-methoxybenzaldehyde in Petasites fragrans? Pollinator-attractant and ant-repellent. Arthropod-Plant Interactions 2017;11(5):623-627.

[344] Senthilkumar A, Venkatesalu V. Chemical composition and larvicidal activity of the essential oil of Plectranthus amboinicus against Anopheles stephensi: a malaria vector mosquito. Parasitology Research 2010;107(5):1275-1278.

[345] Arumugam G et al. Plectranthus amboinicus: Botanical, phytochemical, pharmacological and nutritional significance. Molecules 2016;21:369.

[346] Demarne FE, van der Walt JJA. Pelargonium tomentosum: A potential source of peppermint-scented essential oil. South African Journal of Plant and Soil 1990;7(1):36-39.

[347] Bedoukian Research Inc., 6 Commerce Drive, Danbury, CT 06810, USA. https://bedoukian.com/

[348] Martin B, Etievant P, Henry R. The chemistry of sotolon: A key parameter for the study of a key component of FL or sherry wins. In: Thomas AF, Bessière Y, editors. 6th Congrès Weurman. Chichester: Wiley; 1990; 53-56.

[349] Felix Buccellato. Custom Essence Incorporated, Somerset, NJ USA. Private publication.

[350] Radulovic NS et al. A GC/MS profile of the volatile constituents of the aerial parts of Artemisia abrotanum from Serbia. S Afr J Chem 2009;62:30-32.

[351] Muangphrom P et al. Identification and characterization of (+)-alpha-bisabolol and 7-epi-silphiperfol-5-ene synthases from Artemisia abrotanum. Phytochemistry 2019;164:144-153.

[352] Paqyette LA et al. Total synthesis of (-)-silphiperfol-6-ene and (-)-5-oxosilphiperfol-6-ene. J Am Chem Soc 1984;106:6690-6693.

[353] Dötterl S et al. Nursery pollination by a moth in Silene latifolia: The role of odours in eliciting antennal and behavioural responses. New Phytologist 2006;169:707-718.

[354] https://hort.purdue.edu/newcrop/morton/guava.html

[355] Steinhaus M, Schieberle P et al. Characterization of the key aroma compounds in pink guava (Psidium guajava) by means of aroma re-engineering experiments and omission tests. J Agric Food Chem 2009;57(7):2882-2888.

[356] Radulovic N et al. Composition of diethyl ether flower extracts of Lonicera fragrantissima.
Nat Prod Commun 2009;4(0):1-4.

[357] Wang Y, Lin J. Gas chromatography-olfactometry and gas chromatography-tandem mass spectrometry analysis of fresh cantaloupe (Cucumis melo var. cantalupensis) aroma. Flavour Fragr J 2014;29(2):87-94.

[358] Groth I, Bergström G, Pellmyr O. Floral fragrances in Cimicifuga: Chemical polymorphism and incipient speciation in Cimicifuga simplex. Biochem Syst Ecol 1987;15:441-444.

[359] Napoli E, Dattilo S, Ruberto G. Hydrodistillation of Trachelospermum jasminoides flowers. An analysis of essential oil, hydrolate and polyphenols content of the process wastes. J Essent Oil Res 2020;32(6):556-561.

Additional literature

Calkin RR, Jellinek JS. Perfumery. Practice and principles. New York: John Wiley & Sons, Inc.; 1994.

Arctander S. Perfume and flavor chemicals (aroma chemicals). Las Vegas, NV: Steffen Arctander's Publications; 1969.

Arctander S. Perfume and flavor materials of natural origin. Elisabeth, NJ: Published by the author; 1960.

De Wit HC. Plants of the world, Vol. 1-3. New York: E.P. Dutton & Co. Ltd.; 1966.

Attenborough D. The private life of plants. Jersey: David Attenborough Productions Ltd.; 1995.

 
Links

Eden Botanicals

Leffingwell & Associates

Gernot Katzer's Spice Pages, Institut für Chemie, Strassoldogasse 10, A-8010, Austria.

Musée International de la Parfumerie, Grasse


Agricultural Research Service, United States Department of Agriculture

Purdue University, West Lafayette, IN 47907 USA

Burdocks's Handbook of Flavor Ingredients

www.essentialoils.org

Cropwatch, an independent watchdog for endangered and vulnerable natural aromatic products used in the aroma (perfumes, flavours, aromatherapy, cosmetics), herbal, traditional medicine and phytochemical industries.

 
Photos

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