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Catalyst-Free, Regioselective Ring Opening of Donor-Acceptor Cyclopropanes: Synthesis of Functionalized Mono- and Disulfides

Gopinath, Purushothaman and Chandrasekaran, Srinivasan (2016) Catalyst-Free, Regioselective Ring Opening of Donor-Acceptor Cyclopropanes: Synthesis of Functionalized Mono- and Disulfides. In: SYNTHESIS-STUTTGART, 48 (18). pp. 3087-3096.

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Official URL: http://dx.doi.org/10.1055/s-0035-1561629

Abstract

Interesting sulfur compounds such as monosulfides, symmetrical disulfides, unsymmetrical disulfides, and other 1,3-bifunctionalized compounds were synthesized using benzyltriethylammonium tetrathiomolybdate, BnNEt3](2)MoS4, as the sulfur transfer reagent via regioselective ring opening of donor-acceptor cyclopropanes without the addition of any catalyst.

Item Type: Journal Article
Additional Information: Copy right for this article belongs to the GEORG THIEME VERLAG KG, RUDIGERSTR 14, D-70469 STUTTGART, GERMANY
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Depositing User: Id for Latest eprints
Date Deposited: 28 Oct 2016 07:20
Last Modified: 28 Oct 2016 07:20
URI: http://eprints.iisc.ac.in/id/eprint/55158

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