A Tandem Sulfur Transfer/Reduction/Michael Addition Mediated by Benzyltriethylammonium Tetrathiomolybdate

Prabhu, Kandikere Ramaiah and Sivanand, Pennadam S and Chandrasekaran, Srinivasan (2000) A Tandem Sulfur Transfer/Reduction/Michael Addition Mediated by Benzyltriethylammonium Tetrathiomolybdate. In: Angewandte Chemie, 39 (23). pp. 4316-4319.

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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:	Journal Article
Publication:	Angewandte Chemie
Publisher:	WILEY-VCH Verlag GmbH, Weinheim
Additional Information:	The copyright belongs to WILEY-VCH Verlag GmbH, Weinheim.
Keywords:	Michael additions;Molybdenum;Redox Chemistry;Sulfur;Synthetic methods
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	28 Mar 2006
Last Modified:	19 Sep 2010 04:24
URI:	http://eprints.iisc.ac.in/id/eprint/5616

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