SYNTHESIS OF BOTH ENANTIOMERS OF "ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE, THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE

被引：30

作者：

SATO, T ^{[1
]}

WATANABE, M ^{[1
]}

HONDA, N ^{[1
]}

FUJISAWA, T ^{[1
]}

机构：

[1] MIE UNIV, CHEM DEPT RESOURCES, TSU, MIE 514, JAPAN

来源：

CHEMISTRY LETTERS | 1984年 / 07期

关键词：

D O I：

10.1246/cl.1984.1175

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1175 / 1176

页数：2

共 12 条

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[5] LAURENCE BR, 1982, J CHEM SOC CHEM COMM, P59, DOI 10.1039/c39820000059
[6] STEREOSPECIFIC UMPOLUNG ALPHA-' SUBSTITUTION OF KETONES VIA REACTIONS OF ORGANOCUPRATES WITH ENOL ETHERS OF ALPHA,BETA-EPOXYCYCLOHEXANONES
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[7] ENANTIOSPECIFIC SYNTHESIS OF (+)-ERYTHRO-(5S,6R)-6-ACETOXY-5-HEXADECANOLIDE, AN OPTICALLY-ACTIVE FORM OF THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE
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[8] PHERONE SYNTHESIS .36. SYNTHESIS OF RACEMIC AND OPTICALLY-ACTIVE FORMS OF LINEATIN, THE UNIQUE TRICYCLIC PHEROMONE OF TRYPODENDRON-LINEATUM (OLIVIER)
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[9] PHEROMONE SYNTHESIS .59. SYNTHESIS OF BOTH THE ENANTIOMERS OF ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE - THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE
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[10] STEREOSELECTIVE TOTAL SYNTHESIS OF (4S)-TRANS-BETA-ELEMENONE FROM (S)-2-CYCLOHEXEN-1-OL
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