4.4 Article

Expeditious amide-forming reactions using thiol esters

Journal

TETRAHEDRON LETTERS
Volume 41, Issue 5, Pages 591-594

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(99)02132-2

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The reaction of a 2-pyridylthiol ester with a dimethylaluminum amide leads to the rapid formation of the corresponding amide. The tolylthiol esters can be activated with silver trifluoroacetate and coupled even with poorly reactive amino compounds. (C) 2000 Elsevier Science Ltd. All rights reserved.

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