SYNTHESIS AND BIOLOGICAL ACTIVITY OF OPTICALLY ACTIVE FORMS OF (E)-3,7-DIMETHYL-2-OCTENE-1,8-DIOLIC ACID (CALLOSOBRUCHUSIC ACID); A COMPONENT OF THE COPULATION RELEASE PHEROMONE (ERECTIN) OF THE AZUKI BEAN WEEVIL

DOI: 10.1016/S0040-4020(01)91957-X

Source and publish data:

Tetrahedron p. 2303 - 2306 (1983)

Update date:2022-08-05

Topics:

Authors:

Mori, Kenji

Ito, Teruhito

Tanaka, Kaoru

Honda, Hiroshi

Yamamoto, Izuru

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4020(01)91957-X

Both enantiomers of callosobruchusic acid were synthesized, confirming its proposed plane structure as (E)-3,7-dimethyl-2-octene-1,8-dioic acid.Both of them were biologically active as the copulation release pheromone of Callosobruchus chinensis L.

Full text of DOI:10.1016/S0040-4020(01)91957-X

Products guided by the article

Product name:methyl (E)-6-tosyloxy-3-methyl-2-hexenoate

Cas No:87131-45-1

R&D Labs maybe for 87131-45-1

Hangzhou Yanshan Chemical Co.,Ltd.

Contact:86-571- 87698076

Address:Room 1001, #1 Building, Zhongtian MCC, No.2 Youzhinong, Wenyi West Road, Xihu District, Hangzhou, China
Weifang Ocean Trading Co., Ltd.

Contact:+86-536-2081155

Address:Room2606, Yuqing Building, 518#, Yuquan Road, High-tech Development Zone, Weifang City, Shandong Province, China
Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Hubei anhuang chemical Co.Ltd

Contact:

Address:308# dongwu avenue dongxihu district wuhan city
WD Silicone Co., Ltd

Contact:+86-27-87204219, +86-27-87215023

Address:2402, HuiGu Space-time Building, 8 Forest Road, East Lake Hi-Tech Development Zone

Relevant to this article

Cytotoxic activity and DNA-binding properties of xanthone derivatives

Doi:10.1007/s10895-010-0680-7
(2010)
Application of the palladium(0)-catalyzed ullmann cross-coupling reaction in a total synthesis of (±)-aspidospermidine and thus representing an approach to the lower hemisphere of the binary indole-indoline alkaloid vinblastine

Doi:10.1071/CH05181
(2005)
Enantio- and Regioselective Ir-Catalyzed Hydrogenation of Di- and Trisubstituted Cycloalkenes

Doi:10.1021/jacs.6b07291
(2016)
Doi:10.1097/00004397-200201000-00004
(1929)
Matrix screening of substituted N-aryl-1,8-naphthalimides reveals new dual fluorescent dyes and unusually bright pyridine derivatives

Doi:10.1021/jo050157f
(2005)
An Efficient and Stereocontrolled Synthesis of the Nephritogenoside Core Structure

Doi:10.1016/0040-4039(91)80430-E
(1991)

Article Doi