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

相关论文

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FRATER, G
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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)
FRATER, G
[J]. HELVETICA CHIMICA ACTA, 1979, 62 (08) : 2829 - 2832
[4] KRAUS GA, 1977, TETRAHEDRON LETT, P4575
[5] PREPARATION FOR ERYTHRO-2-HYDROXY-SUCCINIC ACID-DERIVATIVES FROM MALIC ESTERS
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[J]. HELVETICA CHIMICA ACTA, 1980, 63 (01) : 197 - 200
[6] TERASHIMA S, 1979, TETRAHEDRON LETT, P3469
[7] YOSHIOKA H, 1979, TETRAHEDRON LETT, P3489