Chemistry of Insect Antifeedants from Azadirachta indica, Part 14: Absolute Configuration of Azadirachtin

DOI: 10.1039/c39920001304

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1304 - 1306 (1992)

Update date:2022-08-04

Topics:

Authors:

Ley, Steven V.

Lovell, Helen

Williams, David J.

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

Article abstract of DOI:10.1039/c39920001304

The absolute configuration of the insect antifeedant azadirachtin is determined by high field NMR application of the Mosher method and confirmed by X-ray crystallographic analysis.

Full text of DOI:10.1039/c39920001304

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:C₂₉H₃₃F₃O₁₂

Cas No:145415-45-8

R&D Labs maybe for 145415-45-8

Shandong Xiangde Biotechnology Co., Ltd

Contact:+86 -15066639877

Address:Sanba street
Win-Win chemical Co.Ltd

website:http://www.win-winchemical.com

Contact:0086-577-64498589

Address:6F, No. 396 Xingping Road, Longwan Industrial Zone, Wenzhou City, Zhejiang, 325000 P.R.China
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
JiYi Chemical (Beijing) Co., Ltd.

Contact:+86-10-89385733

Address:Shilou Town of Fangshan District， Beijing
Ji'an Hairui Natural Plant Co. Ltd.

Contact:0796-8105528

Address:Meilin industry park, Qingyuan district Ji'an City, Jiangxi Province

Relevant to this article

A novel base-induced isomerization gives access to unprecedented (E)-exo-glycals

Doi:10.1002/chem.201300969
(2013)
Synthesis of fused-β-lactams through selective gold-catalyzed oxycyclization of dioxolane-tethered enynes

Doi:10.1021/jo401390k
(2013)
Synthesis and biological evaluation of prodigiosene conjugates of porphyrin, estrone and 4-hydroxytamoxifen

Doi:10.1016/j.bmc.2013.07.042
(2013)
Synthesis and Pharmacological Evaluation of Selective Histone Deacetylase 6 Inhibitors in Melanoma Models

Doi:10.1021/acsmedchemlett.7b00223
(2017)
Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids

Doi:10.1021/ja407410b
(2013)
SOME NEW ANALOGUES OF VERAPAMIL AND MEPAMIL. SYNTHESIS AND BASIC PHARMACOLOGICAL PROPERTIES

Doi:10.1135/cccc19921967
(1992)

Article Doi