1,2-ADDITION OF SULFUR NUCLEOPHILES TO THE N-ACYLATED IMINE LINKAGE - A MODEL STUDY FOR THE INCORPORATION OF SULFUR NUCLEOPHILES DURING METABOLISM OF ACYLATED AROMATIC-AMINES

被引：6

作者：

CLARK, WM ^{[1
]}

SWENTON, JS ^{[1
]}

机构：

[1] OHIO STATE UNIV,DEPT CHEM,120 W 18TH AVE,COLUMBUS,OH 43210

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1990年 / 55卷 / 13期

关键词：

D O I：

10.1021/jo00300a002

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

: The imine linkage of an acylated quinone imine ketal reacts with ethanethiol to afford an isolable addition product which subsequently rearranges by a facile 1,2-shift to afford an ortho-substituted aromatic amide. © 1990, American Chemical Society. All rights reserved.

引用

页码：3969 / 3971

页数：3

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