SYNTHESIS OF OXAZOLIDINE DERIVATIVES OF BETA-[3-(ARYLOXY)ARYL]-ALPHA-AMINO ACIDS BY APPLICATION OF THE DIELS-ALDER REACTION

被引：11

作者：

OLSEN, RK

FENG, XQ

机构：

[1] Department of Chemistry and Biochemistry, Utah State University Logan

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 41期

关键词：

DIELS-ALDER; ALPHA-AMINO ACIDS; DIARYL ETHER; OXAZOLIDINE; SYNTHESIS;

D O I：

10.1016/S0040-4039(00)93539-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Diels-Alder reaction has been used to construct the diaryl ether unit in oxazolidine derivatives of beta-[3-(aryloxy)aryl]-alpha-amino acids. Cycloaddition of acetylenic ketone 6 with substituted aryloxy dienes, and subsequent aromatization, provided the title compounds in good yields. Reaction of 6 with Danishefsky's diene furnished optically pure derivatives of L-tyrosine.

引用

页码：5721 / 5724

页数：4

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