ChemInform Abstract: Selective Reductions of Conjugated Acetylenes with Magnesium in Methanol and Methanol‐d

Abstract

Peer reviewed

R. O. Hutchins, SUCHISMITA Suchismita, R. E. Zipkin, I. M. Taffer, R. Sivakumar, A. Monaghan and E. M. Elisseou

ChemInform, v 20(29)

18 Jul 1989

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carboxylic acid esters (acyclic compounds)

labeling reactions, deuteration

polyphenylalkene derivatives (stilbene derivatives)

reduction, hydrogenation

The acetylenecarboxylates (I) are reduced with magnesium in methanol to form the saturated esters (II).

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Title: ChemInform Abstract: Selective Reductions of Conjugated Acetylenes with Magnesium in Methanol and Methanol‐d
Creators: R. O. Hutchins - Drexel University
SUCHISMITA Suchismita - Drexel University
R. E. Zipkin - Orthopaedic Research Laboratories
I. M. Taffer - Drexel University, Biology
R. Sivakumar
A. Monaghan
E. M. Elisseou
Publication Details: ChemInform, v 20(29)
Publisher: WILEY‐VCH Verlag GmbH
Number of pages: 1
Resource Type: Abstract
Language: English
Academic Unit: Biology; College of Arts and Sciences
Other Identifier: 991021893410804721