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Merck
  • Solid-phase synthesis of benzisothiazolones as serine protease inhibitors.

Solid-phase synthesis of benzisothiazolones as serine protease inhibitors.

Bioorganic & medicinal chemistry letters (1999-04-14)
K L Yu, R Civiello, D G Roberts, S M Seiler, N A Meanwell
摘要

An efficient solid-phase synthesis of benzisothiazolone-1,1-dioxide-based serine protease inhibitors involving alkylation of carboxylic acids with N-(bromomethyl)benzisothiazolone-1,1-dioxide has been developed. An example using this procedure for preparation of a library of human mast cell tryptase inhibitors is described.

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Sigma-Aldrich
噻霉酮, 97%
Supelco
噻霉酮, analytical standard