REARRANGEMENTS IN LEWIS ACID-CATALYZED DIELS-ALDER REACTIONS - ROUTE TO SUBSTITUTED BICYCLO[2.2.1]HEPTANONES

被引：32

作者：

BALDWIN, JE

LUSCH, MJ

机构：

[1] Chemistry Department, Massachusetts Institute of Technology, Cambridge

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 12期

关键词：

D O I：

10.1021/jo01326a006

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Dieis-Alder adducts of 2, 3-disubstituted butadienes and methacrolein were smoothly rearranged with SnCl4 to substituted bicyclo[2.2.1]heptanones. The structures of the products have been examined, and the scope of this reaction has been investigated. © 1979, American Chemical Society. All rights reserved.

引用

页码：1923 / 1927

页数：5

共 20 条

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