Download 13C-NMR of Natural Products, Volume 1: Monoterpenes and by Atta-Ur-Rahman, V.U. Ahmad PDF

By Atta-Ur-Rahman, V.U. Ahmad

Advances in common product chemistry have resulted in a great number of medications, either derived from medicinal crops, marine crops, and animals, and created as man made analogues of those resources. This ground-breaking, finished quantity offers the newest information at the 13C-NMR of monoterpenes and sesquiterpenes.

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Extra resources for 13C-NMR of Natural Products, Volume 1: Monoterpenes and Sesquiterpenes

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McConnell and W. Fenical, J. Org. , 45(17), 3401 (1980). 49 2-CHLORO-1, 6(~*)-DIBROMO-3(8) (~)-OCH TOOEN-4(R *)-OL Source: Ochtodes crockeri Setchell and Gard ner Mol. formula: C10H15Br2ClO Mol. J. J. McConnell and W. Fenical, J. Org. , 45(17), 3401 (1980). i 1111111111111111111111 111111111111111111111111 ! 111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111 OCHTOOENE Source: Ochtodes secundiramea (Montagne) Howe Mol. formula: C10H14Br2Cl2 Mol. J. McConnell and 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. formula: C16H2408 Mol. 1 H 0. Sticher and 0. Salama, Helv. Chim. Acta, 64(1), 78 (1981).

Formula: C10H14Br2Cl2 Mol. J. McConnell and W. Fenical, J. Org. , 43(21), 4238 (1978). 50 IRIDOID Basic skeleton: 11 7 10 1I11111111111111111111I1111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111III dl-IRIDOMYRMECIN Source: Iridomyrmex humilis Mol. formula: CI0H1602 Mol. 2 P. A. Grieco and C. V. Srinivasan, J. Org. , 46 (12), 2591 (1981). A. Mey) G. Beck. Mol. formula: C9H14°4 Mol. 0 HO-- H. Kobayashi. H. Karasawa.

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