Enantioselective Synthesis of (+)-Quebrachamine using L-Glutamic Acid as a Chiral Template

DOI: 10.1039/c39800000616

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 616 - 617 (1980)

Update date:2022-08-03

Topics:

Authors:

Takano, Seiichi

Chiba, Kenji

Yonaga, Masahiro

Ogasawara, Kunio

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

Article abstract of DOI:10.1039/c39800000616

(+)-Quebrachamine (1) has been synthesised enantioselectively using L-glutamic acid as a chiral template.

Full text of DOI:10.1039/c39800000616

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

View Article Online

Products guided by the article

Product name:(3S,5S)-3-Allyl-3-ethyl-5-hydroxymethyl-dihydro-furan-2-one

Cas No:75652-67-4

R&D Labs maybe for 75652-67-4

Haitong Chemical Industrial Co.,Ltd.

website:https://www.haitonglongwin.com/

Contact:+86-022-66221018

Address:18-701, No.99, The 4th Street, TEDA,
Shanghai Gsyn Chemical Co.,Ltd.

Contact:86-021-67158290

Address:86-021-67158291
Jiaxing Barton Chemicals

website:http://www.chinabarton.com

Contact:+86-573-82719618

Address:No. 162 Fumin Road, Honghe Town,
Sinochem Jiangsu Co.,Ltd.

Contact:86-25-51817806

Address:No. 216, middle longpan road, jincheng tower, floor 21-22, nanjing ,china
chengdu firsterchem Pharmaceutical Co., Ltd.

Contact:028-66825849

Address:chengdu

Relevant to this article

Synthesis and antitubercular activity of lipophilic moxifloxacin and gatifloxacin derivatives

Doi:10.1016/j.bmcl.2007.07.073
(2007)
A ligand influence on the stability of heterobimetallic complexes containing the Ti(μ-O)Al skeleton. Transformation of heterometallic systems to the homometallic Ti(IV) and Al(III) complexes

Doi:10.1039/b710470g
(2007)
Synthesis and conformation of multi-vicinal fluoroalkane diastereoisomers

Doi:10.1002/anie.200701988
(2007)
Reactivity and Diastereoselectivity of Grignard Reagents towards the Hydrazone Functionality in Toluene Solvent

Doi:10.1021/jo00043a001
(1992)
Intramolecular hydroamination of difluoropropargyl amides: Regioselective synthesis of fluorinated β- and γ-lactams

Doi:10.1021/ol701811z
(2007)
Design, synthesis, biological evaluation and molecular docking study of novel thieno[3,2-d]pyrimidine derivatives as potent FAK inhibitors

Doi:10.1016/j.ejmech.2019.112024
(2020)

Article Doi