An example of a chiral non-racemic carbanion as versatile synthon in the asymmetric synthesis of polysubstituted γ-lactones

DOI: 10.1016/S0040-4039(00)79594-3

Source and publish data:

Tetrahedron Letters p. 3039 - 3042 (1992)

Update date:2022-08-04

Topics:

Authors:

Rodriguez

Ramirez Ramirez

Martin Martin

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

Article abstract of DOI:10.1016/S0040-4039(00)79594-3

The application of a chiral non-racemic carbanion generated from enantiomerically enriched α-sulfonyl-γ-lactones to the asymmetric synthesis of highly substituted and fused γ-lactones is described.

Full text of DOI:10.1016/S0040-4039(00)79594-3

Products guided by the article

Product name:Methyl (3S,4R,5R)-3-<3-(benzenesulfonyl)-4-<(methoxycarbonyl)methyl>-2-oxo-5-propyltetrahydrofuran-3-yl>propionate

Cas No:142968-36-3

R&D Labs maybe for 142968-36-3

Wuhan Fortuna Chemical Co.,Ltd

website:http://www.fortunachem.com

Contact:86-27-59207850

Address:Add: Room 2015, No.2 Building, Kaixin Mansion No.107 Jinqiao Avenue, Wuhan, China
Beijing Mediking Biopharm Co., Ltd.

Contact:+86-10-89753524/81760121/81769521

Address:Hongxianghong Incubator, Beiqijia Town, Changping district, Beijing, China
Zhengzhou HQ Material Co.,Ltd

Contact:+86-371-67759225

Address:No.32, Jinsuo Road, High-tech Zone
Aminodiscovery Co.,Ltd.

Contact:+86-535-8888888

Address:No.161 Haishi Rd.
Shandong Xinke Petrochemical Co., Ltd.

Contact:+86-546-7277016

Address:Gudao Industrial Park, Hekou District, Dongying, Shandong Province, China

Relevant to this article

Tataricins A and B, two novel cyclotetrapeptides from Aster tataricus, and their absolute configuration assignment

Doi:10.1016/j.tetlet.2012.12.111
(2013)
Catalytic C-Se bond formation under very mild conditions for the two-step, one-pot synthesis of aryl selenoacetates

Doi:10.1002/adsc.201200486
(2012)
Practical and Efficient Synthesis of 2-Thio-imidazole Derivative - ZY12201: A Potent TGR5 Agonist

Doi:10.1021/acs.oprd.0c00234
(2020)
Regioselective and reductive cleavage of allyl ethers by NaBH ₄-HOAc

Doi:10.1016/j.tet.2013.03.020
(2013)
Understanding the mechanism of the asymmetric propargylation of aldehydes promoted by 1,1′-Bi-2-naphthol-derived catalysts

Doi:10.1021/ja3122137
(2013)
Synthesis of 11-cis-retinoids by hydrosilylation-protodesilylation of an 11,12-didehydro precursor: Easy access to 11- and 12-mono- and 11,12-dideuteroretinoids

Doi:10.1002/chem.201202260
(2012)

Article Doi