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Synthesis 2016; 48(18): 3087-3096
DOI: 10.1055/s-0035-1561629
DOI: 10.1055/s-0035-1561629
paper
Catalyst-Free, Regioselective Ring Opening of Donor–Acceptor Cyclopropanes: Synthesis of Functionalized Mono- and Disulfides
Further Information
Publication History
Received: 24 February 2016
Accepted after revision: 04 April 2016
Publication Date:
13 May 2016 (online)
Abstract
Interesting sulfur compounds such as monosulfides, symmetrical disulfides, unsymmetrical disulfides, and other 1,3-bifunctionalized compounds were synthesized using benzyltriethylammonium tetrathiomolybdate, [BnNEt3]2MoS4, as the sulfur transfer reagent via regioselective ring opening of donor–acceptor cyclopropanes without the addition of any catalyst.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1561629.
- Supporting Information
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