ONE-POT DIELS-ALDER REACTION OF N-P-TOSYLALDIMINES GENERATED BY BF3-ET(2)O CATALYZED TRANSFORMATION OF NAPHTHO[1,8-DE]DITHIIN-1-N-P-TOSYLSULFILIMINES

被引：0

作者：

FUJII, T ^{[1
]}

KIMURA, T ^{[1
]}

FURUKAWA, N ^{[1
]}

机构：

[1] UNIV TSUKUBA,DEPT CHEM,TSUKUBA,IBARAKI 305,JAPAN

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 27期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Naphtho[1,8-de]dithiin-1-N-p-tosylsulfilimines (4) were prepared by the reaction of naphtho[1,8-de]dithiin with chloramine-T. Treatment of 4 with dienes in the presence of BF3-Et(2)O afforded the imino Diels-Alder products via N-p-tosylaldimines produced in situ.

引用

页码：4813 / 4816

页数：4

共 10 条

[1] PREPARATION OF N-P-TOSYLALDIMINES BY THE INTRAMOLECULAR PHOTO-IMINO GROUP MIGRATION OF NAPHTHO[1,8-DE]DITHIIN-1-N-TOSYLSULFILIMINES
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[10] p-Toluenesulfonic acid-catalyzed metal-free formal [4+1] heteroannulation via N-H/O-H/S-H functionalization: One-pot access to 2-aryl/hetaryl/alkyl benzazole derivatives
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