Efficient synthesis of N-acylarenesulfenamides by acylation of arenesulfenamides

被引：18

作者：

Bao, M

Shimizu, M

Shimada, S

Tanaka, M

机构：

[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan

[2] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan

来源：

TETRAHEDRON | 2003年 / 59卷 / 03期

关键词：

acylation; sulfenamides; amides; acid chlorides; imidic acids;

D O I：

10.1016/S0040-4020(02)01554-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Acylation of arenesulfenamides proceeds efficiently by using either perfluorocarboxylic anhydrides or acid chlorides in the presence of pyridine as a base at low temperatures to give N-acylarenesulfenamides. Some N-alkylcarbonyl derivatives exist with imidic acid tautomers in an aprotic solvent. (C) 2003 Elsevier Science Ltd. All rights reserved.

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收藏

页码：303 / 309

页数：7

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