SYNTHESIS AND ENANTIOMERIC PURITY DETERMINATION OF THE OPTICALLY-ACTIVE EPOXIDE DISPARLURE, SEX-PHEROMONE OF THE GYPSY-MOTH

被引：42

|

作者：

PIRKLE, WH

RINALDI, PL

机构：

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 07期

关键词：

D O I：

10.1021/jo01321a001

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：1025 / 1028

页数：4

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[33] SEX-PHEROMONE OF THE EUROPEAN GRAPEVINE MOTH, LOBESIA-BOTRANA SCHIFF. (LEPIDOPTERA, TORTRICIDAE) - SYNTHESIS AND EFFECT OF ISOMERIC PURITY ON BIOLOGICAL-ACTIVITY
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[34] SYNTHESIS OF OPTICALLY-ACTIVE 2-(1-NAPHTHYL)-BUTANE - DETERMINATION OF ABSOLUTE-CONFIGURATION AND OPTICAL PURITY
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[35] SYNTHESIS OF THE 3 ACTIVE COMPONENTS OF THE SEX-PHEROMONE OF THE MASSON PINE CATERPILLAR MOTH-(Z,E)-5, 7-DODECADIEN-1-OL, ACETATE AND PROPIONATE
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[36] PHEROMONE SYNTHESIS .86. SYNTHESES OF OPTICALLY-ACTIVE PHEROMONES WITH AN EPOXY RING, (+)-DISPARLURE AND BOTH THE ENANTIOMERS OF (3Z,6Z)-CIS-9,10-EPOXY-3,6-HENEICOSADIENE
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[37] ABSOLUTE-CONFIGURATION OF CIS, TRANS 1,5-CYCLOOCTADIENE - DETERMINATION OF ENANTIOMERIC PURITY WITHOUT KNOWLEDGE OF MAXIMUM OPTICAL-ROTATION AND WITHOUT AID OF AN AUXILIARY OPTICALLY-ACTIVE SUBSTANCE
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[38] OPTICALLY-ACTIVE, AROMATIC SPIRANES .5. STEREOCHEMISTRY OF METALLOCENES .39. UNIVERSAL METHOD FOR PREPARATION, AND DETERMINATION OF ABSOLUTE-CONFIGURATION AND ENANTIOMERIC PURITY OF CHIRAL 2,2'-SPIROBIINDANES
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[39] STUDIES ON THE IDENTIFICATION AND SYNTHESES OF INSECT PHEROMONES .20. SYNTHESIS OF (7R, 8S)-(+)-SEX PHEROMONE OF GYPSY-MOTH ACCORDING TO KINETIC RESOLUTION OF (+1) ALLYLIC ALCOHOL BY SHARPLESS ASYMMETRIC EXPOXIDATION
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[40] OPTICALLY-ACTIVE TRANS-BIS(HYDROXYDIPHENYLMETHYL)-2,2-DIMETHYL-1,3-DIOXACYCLOPENTANE AND ITS DERIVATIVES AS CHIRAL SHIFT-REAGENTS FOR THE DETERMINATION OF ENANTIOMERIC PURITY AND ABSOLUTE-CONFIGURATION
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