The aza-Diels-Alder reaction protocol -: a useful approach to chiral, sterically constrained α-amino acid derivatives

被引：23

作者：

Bertilsson, SK ^{[1
]}

Ekegren, JK ^{[1
]}

Modin, SA ^{[1
]}

Andersson, PG ^{[1
]}

机构：

[1] Uppsala Univ, Inst Chem, Dept Organ Chem, SE-75121 Uppsala, Sweden

来源：

TETRAHEDRON | 2001年 / 57卷 / 30期

关键词：

oc-amino acid; aza-Diels-Alder reaction; anthracene; tetrahydroquinoline;

D O I：

10.1016/S0040-4020(01)00531-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Different types of polycyclic alpha -amino acid derivatives are prepared from chiral imines by using well-established aza-Diels-Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15-21 are formed. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：6399 / 6406

页数：8

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