A tandem sulfur transfer/reduction/michael addition mediated by benzyltriethylammonium tetrathiomolybdate

Prabhu, Kandikere Ramaiah ; Sivanand, Pennadam S. ; Chandrasekaran, Srinivasan (2000) A tandem sulfur transfer/reduction/michael addition mediated by benzyltriethylammonium tetrathiomolybdate Angewandte Chemie, 112 (23). pp. 4486-4489. ISSN 0044-8249

Full text not available from this repository.

Official URL: http://www3.interscience.wiley.com/journal/7650085...

Related URL: http://dx.doi.org/10.1002/1521-3757(20001201)112

Abstract

Disulfides and sulfur containing organic compounds are important functional groups widely present in nature and have commercial significance.[1] Therefore, the synthesis of disulfides, sulfides, and w-thioketones is not only attractive but also finds numerous applications.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons, Inc.
ID Code:7158
Deposited On:25 Oct 2010 12:26
Last Modified:01 Feb 2011 11:32

Repository Staff Only: item control page