The chemistry of 2H-3,1-benzoxazine-2,4(1H)-dione (isatoic anhydride).: XXIV.: N-benzylation of isatoic anhydride under Mitsunobu conditions

被引：4

作者：

Coppola, GM ^{[1
]}

机构：

[1] Novartis Inst Biomed Res, Dept Metab & Cardiovasc Dis, Summit, NJ 07901 USA

来源：

SYNTHETIC COMMUNICATIONS | 2002年 / 32卷 / 07期

关键词：

D O I：

10.1081/SCC-120003148

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Isatoic anhydride is readily alkylated on nitrogen with benzylic alcohols in the presence of triphenylphosphine and diethyl azodicarboxylate. Both electron donating and electron withdrawing groups are tolerated.

引用

页码：1009 / 1013

页数：5

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