Stereochemistry of (–)-virantmycin
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 2,p. 409-411
- https://doi.org/10.1039/p19900000409
Abstract
The stereochemistry of the antiviral metabolite (–)-virantmycin has been determined by NOE difference spectroscopy to be 2R,3R. This reverses an earlier stereochemical proposal for C-2. NOEs from a slowly exchanging hydroxy proton in a synthetic intermediate provided the key stereochemical information.This publication has 10 references indexed in Scilit:
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