Issue 9, 1985

A 13C and 1H nuclear magnetic resonance study of some diastereoisomeric homoeburnane derivatives

Abstract

Several 14-hydroxy-E-homoeburnane diastereoisomers have been synthesized and studied by 1H and 13C n.m r spectroscopy. The relative configurations and predominating conformations have been established. It has been shown that previous assignments of C-17 and C-20 signals of trans-D/E-ring-fused Vinca alkaloids must be reversed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1985, 1319-1322

A 13C and 1H nuclear magnetic resonance study of some diastereoisomeric homoeburnane derivatives

G. Tóth, C. Szántay, L. Szabó, K. Nógrádi, G. Kalaus and C. Szántay, J. Chem. Soc., Perkin Trans. 2, 1985, 1319 DOI: 10.1039/P29850001319

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