THE STEREOSELECTIVE ALPHA-ALKYLATION OF CHIRAL BETA-HYDROXY ESTERS AND SOME APPLICATIONS THEREOF

被引：267

作者：

FRATER, G

MULLER, U

GUNTHER, W

机构：

来源：

TETRAHEDRON | 1984年 / 40卷 / 08期

关键词：

D O I：

10.1016/S0040-4020(01)82413-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

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页码：1269 / 1277

页数：9

相关论文

共 40 条

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[6] Fr?ter G., 1980, HELV CHIM ACTA, V63, P1383
[7] STEREOSPECIFIC SYNTHESIS OF (+)-(3R,4R)-4-METHYL-3-HEPTANOL - ENANTIOMER OF A PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE (SCOLYTUS-MULTISTRIATUS)
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[J]. HELVETICA CHIMICA ACTA, 1979, 62 (08) : 2829 - 2832
[8] 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
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[J]. TETRAHEDRON LETTERS, 1981, 22 (05) : 425 - 428
[9] FRATER G, UNPUB
[10] FRATER G, 1979, HELV CHIM ACTA, V62, P2827

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