Reductive Cleavage of the Se–Se Bond in the Presence of a Zn/AlCl3 System: Synthesis of Selenol Esters-Reference-Cited by-同舟云学术

Reductive Cleavage of the Se–Se Bond in the Presence of a Zn/AlCl3 System: Synthesis of Selenol Esters

Published:2004-02 Issue:2 Volume:2004 Page:148-149
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Movassagh Barahman¹,Shamsipoor Mojgan¹,Joshaghani Mohammad²

Affiliation:

1. Department of Chemistry, K.N. Toosi University of Technology, PO Box 15875-4416, Tehran Iran

2. Department of Chemistry, Razi University, 67149 Kermanshah, Iran

Abstract

Selenol esters were prepared in good yields by reacting diselenides with carboxylic acid anhydrides in dry acetonitrile in the presence of a Zn/AlCl3 system.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823404323000549

Reference49 articles.

1. Organic Selenium and Tellurium Compounds (1986)

2. Modern organoselenium chemistry

3. SELENIUM AND TELLURIUM ISOLOGUES OF CARBOXYLIC ACID DERIVATIVES

4. Aryl selenocyanates and aryl thiocyanates: reagents for the preparation of activated esters

5. Acyl radicals: functionalized free radicals for intramolecular cyclization reactions

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