By Atta-Ur-Rahman, V.U. Ahmad
Advances in typical product chemistry have resulted in plenty of medicines, either derived from medicinal vegetation, marine vegetation, and animals, and created as artificial analogues of those resources. This ground-breaking, complete quantity provides the newest info at the 13C-NMR of monoterpenes and sesquiterpenes.
Read Online or Download 13C-NMR of Natural Products, Volume 1: Monoterpenes and Sesquiterpenes PDF
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Extra resources for 13C-NMR of Natural Products, Volume 1: Monoterpenes and Sesquiterpenes
L. Simonsen, J. Chern. , 117 (1), 570 (1920). 1I111111111111111I111111111111111111111111111111111111111111111111111I11111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111III FENCHANE Basic skeleton: 10 38 FENCHONE Source: Luvunga scandens Mol. formula: Cl0 H160 Mol. 9 1. E. O. , (23), 1433 (1969). W. Cochran and D. Doddrell, J. Chern. Soc. Chern. 2. K. Baslas. Perfumery Essent. Oil Record, 50, 124 (1959). IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII111111111111111111111111111111111111111111111111111111III lO-HYDROXYFENCHONE Source: Foeniculum vulgare Mol.
Urban and Gilg. 4 Mol. formula: C15H2208 Mol. J. El-Naggar, (1982) . L. W. Doskotch, J. Nat. 1 Mol. formula: C15H2408 Mol. 4 H. Kobayashi, H. Karasawa, T. Miyase and S. Fukushima, Chern. Pharm. Bull. (Tokyo), 33 (9), 3645 (1985). ) Urban and Gilg. 4 Mol. formula: C15 H24 0 8 Mol. J. EI-Naggar, J . L. (1982) . W. Doskotch, J. Nat. 5 Mol. formula: C15H2009 Mol. R. J. Nielsen, Phytochemistry, 24 (3), 602 (1985). 1I11111111 11111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111III BOSCHNALOSIDE Source: Euphpasia saZisbupgensis Hoppe Mol.
Kameoka, Chemistry Express, 2 (9)' 547 (1987). 39 CYCLOCITRAL Basic skeleton: 2 3 7 8 1111 " 1111 " I " " I " " I11111111111111111111 " 11I1 " III " II " II " 11111111 " II " II " I " I " " " " II " II " " II " III " " I " " I " 11111111 " 111111111111111 11111111111 111111 MHTHYL)-2,4,4-TRIMHTHYL-2, 5-CYCLOHEXADIEN-I-ONE 3-(~-D-GLUCOPYRANOSYLOXY Source: Eryngium campestre L. Mol. formula: C16H2407 Mol. J. Erdelmeier and 0. Sticher, Phytochemistry, 25 (3), 741 (1986). 40 METHYL)2,4, 4-TRIMETHYL-2-CYCLOHEXEN-I-ONE 3-(~-D-GLUCOPYRANOSYLOXY Source: Eryngium campestre L.