ON THE STEREOSELECTIVITY OF THE ALPHA-ALKYLATION OF BETA-HYDROXY ESTERS - ENANTIOSELECTIVE SYNTHESIS OF 4,4-DISUBSTITUTED AND 6,6-DISUBSTITUTED CYCLOHEX-2-EN-1-ONES

被引：45
作者：
FRATER, G
机构：
来源：
TETRAHEDRON LETTERS | 1981年 / 22卷 / 05期
关键词：
D O I：
10.1016/0040-4039(81)80116-5
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
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页码：425 / 428
页数：4
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[3]   STEREOSPECIFIC SYNTHESIS OF (+)-(3R,4R)-4-METHYL-3-HEPTANOL - ENANTIOMER OF A PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE (SCOLYTUS-MULTISTRIATUS) [J].
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[5]   PREPARATION FOR ERYTHRO-2-HYDROXY-SUCCINIC ACID-DERIVATIVES FROM MALIC ESTERS [J].
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[6]  
TERASHIMA S, 1979, TETRAHEDRON LETT, P3469
[7]  
YOSHIOKA H, 1979, TETRAHEDRON LETT, P3489
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