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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
要旨

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
ベンジルトリメチルアンモニウムクロリド, 97%
Sigma-Aldrich
ベンジルトリメチルアンモニウムヒドロキシド 溶液, 40 wt. % in H2O
Sigma-Aldrich
ベンジルトリメチルアンモニウムヒドロキシド 溶液, 40 wt. % in methanol
Sigma-Aldrich
ベンジルトリメチルアンモニウムブロミド, 97%
Sigma-Aldrich
ベンジルトリメチルアンモニウムクロリド 溶液, technical, ~60% in H2O