Download 13C-NMR of Natural Products, Volume 2: Diterpenes by Atta-Ur-Rahman, V.U. Ahmad PDF

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

13C-NMR spectroscopy performs an enormous position within the elucidation of natural compound buildings. Chemists studying new compounds will locate this quantity, which covers the 13C-NMR information of diterpenes, a useful reference resource.

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Additional resources for 13C-NMR of Natural Products, Volume 2: Diterpenes

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Formula: C20 H34 0 Mol. : 290 Solvent: CDCl3 1. L. Buckwalter, LR. A. Nagel, E. Wenkert and F. Naf, Helv. Chim. , 58(6), 1567 (1975). 2. G. 38 ohloff , Helv. Chim. , 41(3),845 (1958). HAVARDIOL Source: Grindelia havardii Steyerm. Mol. formula: C19H3202 Mol. D. N. J. B. J. Siahaan, Phytochemistry, 26(2), 483 (1987). lilllllllllllllllllllllllllllllllllllllllllllllllllill111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111III STEREBIN D Source: Stevia rebaudiana Bertoni Mol.

1111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111II RETINOIC ACID Source: Rat liver Mol. formula: C20H2802 Mol. : 300 Solvent: CDCl3+Dioxane 1:1 1. G. Englert, Helv. Chim. Acta, 58 (8), 2367 (1975). 2. S. K. Murthy and J. Ganguly, Biochem. , 85, 326 (1962). 32 AGELASINE E Source: AgeZas nakamur>ai Hoshino Mol. formula: C26H40CIN5 Mol. 0 H. Wu, H. 1. Kobayashi, Y. Ohizumi and Y. , 25 (34), 3719 (1984).

45 2-0XOMANOYL OXIDE Source: Dacrydium colensoi Mol. formula: C20H3202 Mol. 4 1. O. R. W. Wehrli, Acta. Chern. , 29, 695 (1975). 2. R. W. Brandt, Chern. , 68, 286 (1935). 1I1111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111111III 3-0XOMANOYL OXIDE Source: Xylia dolabriformis Mol. formula: C 20 H32 0 2 Mol. : 304 Solvent: CDCl3 1. O. R. W. Wehrli, Acta. Chern. , 29, 695 (1975). 2. A. W. Morgan, J.

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