By J. D. Connolly, R. A. Hill (auth.)

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Additional info for Dictionary of Terpenoids: Volume 1: Mono- and Sesquiterpenoids / Volume 2: Di- and higher Terpenoids / Volume 3: Indexes

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3,5-Dinitrobenzoyl: Mp 60-62°. 1-Naphthylurethane: Mp 76°. Me ether: [626-91-5]. 687. Bp 91°. Et ether: [628-04-6]. 1-Ethoxy-3-methylbutane, 9CI. 200 Substance responsible for "sun-struck" flavour of beer. Liq. with leek-like aroma. 5-127°. Kuroiwa, Y. et al, Agric. Bioi. , 1961, 25, 257 (isol) Obota, Y. G. -C. et al, Arch. Pharm. ), 1976, 309, 1019 (synth) methylbutyl ether. 203 2-Methyl-2-butenoic acid Liq. 764. Bp 112°. , Bull. Soc. Chim. C. eta/, J. Am. Chern. F. , 1975, 3041 (synth) Debal, A.

Nat. , 1979,38,47 21. , Recent Adv. , 1990, 24, 161 22. G. , Prog. Chem. Org. Nat. , 1985,47,153 23. , Prog. Chem. Org. Nat. , 1977, 34,82 24. Bordoloi, M. , Phytochemistry, 1989, 28, 2007 25. , Ace. Chem. , 1981,14, 82; Prog. Chem. Org. Nat. , 1981, 40, 49 26. Murakami, T. , Prog. Chem. Org. Nat. , 1988,50,1 27. A. , Prog. Chem. Org. Nat. , 1974,31,283 28. , Prog. Chem. Org. Nat. , 1971, 29,395 29. R. in Chemistry of Terpenes and Terpenoids, Ed. , Academic Press, London,1972,p. 155 30. A. in Biosynthesis of Isoprenoid Compounds, Ed.

17 18 X Carotenoid end-groups 5. IUPAC treats the 'hydro' prefix as non-detachable. This Dictionary follows IUPAC recommendations for nomenclature except that the 'hydro' prefix is treated as detachable and is placed alphabetically with the other prefixes. CA also uses a detachable 'hydro' prefix but it does not use hypothetical parents such as P-caroten-6-ols which are incapable of existence (see current Chemical Abstracts Index 6. 7. 8. 9. xlviii Ruzicka, L. , Helv. Chim. , Proc. Chern. , 1959, 341 Ruzicka, L.

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