1H and 13C NMR structure determination of a new stereoisomer of isoreserpiline pseudoindoxyl from Rauvolfia grandiflora

Magnetic Resonance in Chemistry
2003.0

Abstract

An NMR study of a new stereoisomer of isoreserpiline pseudoindoxyl alkaloid is described. The complete 1H and 13C NMR assignments of the compound were carried out using COSY, HMQC and HMBC. Stereochemistry at carbons C-2, C-3, C-15, C-20 and C-19 was established using values of 1H chemical shifts, coupling constants and NOESY experiments. © 2003 John Wiley & Sons, Ltd.

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