Stereoselective separation of (1S, 4S )-sertraline from medicinal reaction mixtures by countercurrent chromatography with hydroxypropyl-β-cyclodextrin as stereoselective selector-Reference-Cited by-同舟云学术

Stereoselective separation of (1S, 4S )-sertraline from medicinal reaction mixtures by countercurrent chromatography with hydroxypropyl-β-cyclodextrin as stereoselective selector

Published:2019-06-24 Issue:16 Volume:42 Page:2734-2742
ISSN:1615-9306
Container-title:Journal of Separation Science
language:en
Short-container-title:J. Sep. Sci.

Author:

Sun Wenyu¹,Wang Chaoyue¹,Jin Yang¹,Wang Xiang¹,Zhao Shanshan¹,Luo Meng¹,Yan Jizhong¹,Tong Shengqiang¹^ORCID

Affiliation:

1. College of Pharmaceutical Science; Zhejiang University of Technology; Hangzhou P. R. China

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jssc.201900340/fullpdf

Reference33 articles.

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3. Efficient enantioselective synthesis of sertraline, a potent antidepressant, via a novel intramolecular nucleophilic addition to imine;Chen;Org. Lett.,1999

4. Selective functionalization of 1,2-dihydronaphthalenols leads to a concise, stereoselective synthesis of sertraline;Lautens;Tetrahedron,1999

5. An expedient total synthesis of cis-(+)-Sertraline from D-Phenylglycine;Chandrasekhar;Tetrahedron,2000

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