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

Wuhan Sunrise Pharmaceutical Technology Co., Ltd

Contact:+86-27-83314682

Address:Room 340, New material Industrial base No.17, Gu Tian Five Lu , Qiaokou District, Wuhan , China
Kraeber & Co GmbH

Contact:+49-4101-3053-0

Address:Waldhofstrasse 14 ,25474 Ellerbek Germany
Zhengzhou Xinlian Chemical Tech Co. ,Ltd

Contact:0371-65771781 021-52042910

Address:H Part, Building I, No. 700 Gonglu Road, Pudong New Area, Shanghai
Jiangsu Fengshan Group Co., Ltd.

Contact:86-25-86558671

Address:1903,Central International Mansion 105-6 North Zhongshan Road, Nanjing, China
Chengdu NoVi Biotechnology Co., Ltd.(expird)

Contact:13551243286/028-81458053

Address:NO.168-1-224 JULONG ROAD WUHOU DISTRICT, CHENGDU CITY,SICHUAN PROVINCE

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