Asymmetric synthesis of H1 receptor antagonist (R,R)-clemastine-Reference-Cited by-同舟云学术

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Asymmetric synthesis of H1 receptor antagonist (R,R)-clemastine

Published:2015-07-29 Issue:12 Volume:38 Page:2131-2136
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch. Pharm. Res.

Author:

Lee Sun Young,Jung Jung Wha,Kim Tae-Hyun,Kim Hee-Doo

Funder

Sookmyung Women’s University Research Grants 2012

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12272-015-0641-4.pdf

Reference17 articles.

1. Chang, M., T.H. Kim, and H.D. Kim. 2008. Stereoselective synthesis of (+)-flutriafol. Tetrahedron Asymmetry 19: 1503–1507.

2. Ebnöther, A., and H.P. Weber. 1976. Synthesis and absolute configuration of clemastine and its isomers. Helvetica Chimica Acta 59: 2462–2468.

3. Fernández-Mateos, E., B. Marciá, and M. Yus. 2014. Catalytic enantioselective addition of aryl Grignard reagents to ketones. European Journal of Organic Chemistry 29: 6519–6526.

4. Forrat, V.J., O. Prieto, D.J. Ramón, and M. Yus. 2006. trans-1-Sufonylamino-2-isoborneolsulfonylaminocyclohexane derivatives: Excellent chiral ligands for catalytic enantioselective addition of organozinc reagents to ketones. Chemistry-A European Journal 12: 4431–4445.

5. Fournier, A.M., R.A. Brown, W. Farnaby, H. Miyatake-Ondozabal, and J. Clayden. 2010. Synthesis of (–)-(S,S)-clemastine by invertive N → C aryl migration in lithiated carbamate. Organic Letters 12: 2222–2225.

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