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

被引：90

作者：

MORI, K

EBATA, T

机构：

来源：

TETRAHEDRON | 1986年 / 42卷 / 13期

关键词：

D O I：

10.1016/S0040-4020(01)87314-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3471 / 3478

页数：8

共 27 条

[11] THE 1ST PRACTICAL METHOD FOR ASYMMETRIC EPOXIDATION [J].

KATSUKI, T ;

SHARPLESS, KB .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (18) :5974-5976

[12]

KRAEVSKII AA, 1962, DOKL AKAD NAUK SSSR+, V146, P1349

[13]

LIN GQ, 1984, ACTA CHIM SINICA, P74

[14] SYNTHESIS OF CHIRAL 1,2-DIOLS AND RELATED-COMPOUNDS OF BIOLOGICAL-ACTIVITIES VIA STEPWISE RING FISSION OF 5-ALKYL-6,8-DIOXABICYCLO[3.2.1]OCTANE SKELETON [J].

MASAKI, Y ;

SERIZAWA, Y ;

NAGATA, K ;

ODA, H ;

NAGASHIMA, H ;

KAJI, K .

TETRAHEDRON LETTERS, 1986, 27 (02) :231-234

[15] GYPSY MOTH (LEPIDOPTERA-LYMANTRIIDAE) FIELD TRAPPING AND ELECTROANTENNOGRAM STUDIES WITH PHEROMONE ENANTIOMERS [J].

MILLER, JR ;

MORI, K ;

ROELOFS, WL .

JOURNAL OF INSECT PHYSIOLOGY, 1977, 23 (11-1) :1447-1453

[16] PHEROMONE SYNTHESIS .25. STEREOSELECTIVE SYNTHESIS OF THE BOTH ENANTIOMERS OF DISPARLURE, THE PHEROMONE OF THE GYPSY-MOTH [J].

MORI, K ;

TAKIGAWA, T ;

MATSUI, M .

TETRAHEDRON, 1979, 35 (07) :833-837

[17]

MORI K, 1976, TETRAHEDRON LETT, P3953, DOI 10.1016/S0040-4039(00)92545-0

[18] SYNTHESIS OF OPTICALLY-ACTIVE PHEROMONES WITH AN EPOXY RING, (+)-DISPARLURE AND THE SALTMARSH CATERPILLAR MOTH PHEROMONE [(Z,Z)-3,6-CIS-9,10-EPOXYHENEICOSADIENE] [J].

MORI, K ;

EBATA, T .

TETRAHEDRON LETTERS, 1981, 22 (43) :4281-4282

[19] STEREOCONTROLLED TOTAL SYNTHESIS OF LIPOXINS-A [J].

NICOLAOU, KC ;

VEALE, CA ;

WEBBER, SE ;

KATERINOPOULOS, H .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (25) :7515-7518

[20] UNSATURATED FATTY ACIDS .2. THE SYNTHESIS OF LINOLENIC ACID [J].

NIGAM, SS ;

WEEDON, BCL .

JOURNAL OF THE CHEMICAL SOCIETY, 1956, (NOV) :4049-4054

← 1 2 3 →