Benzyltriethylammonium tetrathiomolybdate: An improved sulfur transfer reagent for the synthesis of disulfides

Article abstract of DOI:10.1080/00397919208021143

Benzyltriethylammonium tetrathiomolybdate has been found to be a superior reagent for the conversion of alkyl halides to the corresponding disulfides in chloroform at room temperature.

Full text of DOI:10.1080/00397919208021143

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Benzyltriethylammon
Tetrathiomolybdate: An
Improved Sulfur Transfer
Reagent for the Synthesis of
Disulfides
A. R. Ramesha a & S. Chandrasekaran a
a Department of Organic Chemistry, Indian Institute
of Science, Bangalore, 560 012, India
Published online: 23 Sep 2006.
To cite this article: A. R. Ramesha & S. Chandrasekaran (1992): Benzyltriethylammon
Tetrathiomolybdate: An Improved Sulfur Transfer Reagent for the Synthesis
of Disulfides, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 22:22, 3277-3284
To link to this article: http://dx.doi.org/10.1080/00397919208021143
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