ATTRACTANCY AND SPECIES SPECIFICITY OF 6-ACETOXY-5-HEXADECANOLIDE, A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE

被引：28

作者：

HWANG, YS ^{[1
]}

MULLA, MS ^{[1
]}

CHANEY, JD ^{[1
]}

LIN, GG ^{[1
]}

XU, HJ ^{[1
]}

机构：

[1] CHINESE ACAD SCI,SHANGHAI INST ORGAN CHEM,SHANGHAI,PEOPLES R CHINA

来源：

JOURNAL OF CHEMICAL ECOLOGY | 1987年 / 13卷 / 02期

关键词：

D O I：

10.1007/BF01025885

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：245 / 252

页数：8

共 8 条

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[2] SYNTHESIS OF THE 2 ENANTIOMERIC FORMS OF "ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE, THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE [J].

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[3] AN OVIPOSITION ATTRACTANT PHEROMONE IN CULEX-QUINQUEFASCIATUS SAY (DIPTERA, CULICIDAE) [J].

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[4] ABSOLUTE-CONFIGURATION OF MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE, 6-ACETOXY-5-HEXADECANOLIDE [J].

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[5]

LAURENCE BR, 1982, J CHEM SOC CHEM COMM, P59, DOI 10.1039/c39820000059

[6]

LIN GQ, 1985, TETRAHEDRON LETT, V26, P1233

[7] PHEROMONE SYNTHESIS .59. SYNTHESIS OF BOTH THE ENANTIOMERS OF ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE - THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE [J].

MORI, K ;

OTSUKA, T .

TETRAHEDRON, 1983, 39 (20) :3267-3269

[8]

Sakakibara M., 1984, Japanese Journal of Sanitary Zoology, V35, P401

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