Issue 3, 1978

2H nuclear magnetic resonance studies on biosynthesis: stereochemistry of the 5′-hydrogen atoms of griseofulvin derived from griseophenone B and 4-demethyldehydrogriseofulvin

Abstract

2 H N.m.r. spectroscopy has been used to establish that in Penicillium urticae, griseofulvin is biosynthesized with the 5′α-configuration of deuterium from [5′-2H]griseophenone B and 4-demethyl-[5′-2H]-dehydrogriseofulvin.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 135-136

2 H nuclear magnetic resonance studies on biosynthesis: stereochemistry of the 5′-hydrogen atoms of griseofulvin derived from griseophenone B and 4-demethyldehydrogriseofulvin

Y. Sato, T. Oda and H. Saitô, J. Chem. Soc., Chem. Commun., 1978, 135 DOI: 10.1039/C39780000135

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements