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  • Synthesis of thioesters from carboxylic acids via acyloxyphosphonium intermediates with benzyltriethylammonium tetrathiomolybdate as the sulfur transfer reagent.

Synthesis of thioesters from carboxylic acids via acyloxyphosphonium intermediates with benzyltriethylammonium tetrathiomolybdate as the sulfur transfer reagent.

The Journal of organic chemistry (2009-07-22)
Purushothaman Gopinath, Ravindran Sasitha Vidyarini, Srinivasan Chandrasekaran
RÉSUMÉ

An efficient protocol is reported for the synthesis of thioesters from carboxylic acids with use of acyloxy phosphonium salts as intermediates and benzyltriethylammonium tetrathiomolybdate as the sulfur transfer reagent.

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Sigma-Aldrich
Benzyltrimethylammonium chloride, 97%
Sigma-Aldrich
Benzyltrimethylammonium hydroxide solution, 40 wt. % in H2O
Sigma-Aldrich
Benzyltrimethylammonium hydroxide solution, 40 wt. % in methanol
Sigma-Aldrich
Benzyltrimethylammonium bromide, 97%
Sigma-Aldrich
Benzyltrimethylammonium chloride solution, technical, ~60% in H2O