Issue 12, 1988

A convenient route to an acetylenic C35 hopanoid and the absolute configuration of the side-chain of aminobacteriohopanetriol

Abstract

The absolute configuration of the side-chain of aminobacteriohopanetriol has been determined as (32R, 33R, 34S) by n.m.r. spectroscopy of its 32,34-O-isopropylidene-N-acetyl derivative and by chemical correlation with bacteriohopanetetrol yielding an acetylenic bacteriohopane intermediate of potential synthetic value.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 830-832

A convenient route to an acetylenic C35 hopanoid and the absolute configuration of the side-chain of aminobacteriohopanetriol

S. Neunlist and M. Rohmer, J. Chem. Soc., Chem. Commun., 1988, 830 DOI: 10.1039/C39880000830

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