THE ENANTIOSELECTIVE CONVERSION OF ORTHO-SUBSTITUTED BENZOIC-ACIDS TO CHIRAL CYCLOHEXANE DERIVATIVES

被引：31
作者：
SCHULTZ, AG
SUNDARARAMAN, P
MACIELAG, M
LAVIERI, FP
WELCH, M
机构：
来源：
TETRAHEDRON LETTERS | 1985年 / 26卷 / 38期
关键词：
D O I：
10.1016/S0040-4039(00)98755-0
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
引用
收藏
页码：4575 / 4578
页数：4
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[3]   ENANTIOSELECTION IN THE BIRCH REDUCTION-ALKYLATION OF A CHIRAL BENZOIC-ACID DERIVATIVE [J].
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[4]   THE INTRAMOLECULAR DIENE-CARBENE CYCLO-ADDITION EQUIVALENCE AND AN ENANTIOSELECTIVE BIRCH REDUCTION ALKYLATION BY THE CHIRAL AUXILIARY APPROACH - TOTAL SYNTHESIS OF (+/-)-LONGIFOLENE AND (-)-LONGIFOLENE [J].
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[5]  
SCHULTZ AG, J ORG CHEM
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SONNET PE, 1980, J ORG CHEM, V45, P3139
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