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

Shanghai Maxchemco Chemical Industry Co., Ltd.

Contact:(86)21-51079223

Address:No.1305-8, B241, the Ecust Park, Huajing Road, Xuhui District, Shanghai
Lishui Nanming Chemical Co., Ltd(expird)

Contact:+86-0578-2134101，2697830

Address:No.19 Tongji Road Shuige Industrial zone
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
Hangzhou Dingyan Chem Co., Ltd

website:http://www.dingyanchem.com

Contact:86-571-87157530

Address:RM.1118,NO.1 Building, Baiyun Tower,Jianggan Area, Hangzhou city, China,310004

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