Issue 7, 1978

Nonoxidative cyclization of squalene by Tetrahymena pyriformis. The incorporation of a 3β-hydrogen (deuterium) atom into tetrahymanol

Abstract

It was shown by 2H-n.m.r. spectroscopy that the proton introduced by T. pyriformis in the cyclization of squalene assumes the 3β-stereochemistry in the biosynthesized tetrahymanol.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 333-334

Nonoxidative cyclization of squalene by Tetrahymena pyriformis. The incorporation of a 3β-hydrogen (deuterium) atom into tetrahymanol

D. J. Aberhart, S. P. Jindal and E. Caspi, J. Chem. Soc., Chem. Commun., 1978, 333 DOI: 10.1039/C39780000333

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