Diastereomeric salts of (<i>S</i>,<i>S</i>)-sertraline with <scp>l</scp>- and <scp>d</scp>-tartaric acids: an investigation into chiral supramolecular discrimination-Reference-Cited by-同舟云学术

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Diastereomeric salts of (S,S)-sertraline with l- and d-tartaric acids: an investigation into chiral supramolecular discrimination

Published:2023 Issue:11 Volume:25 Page:1693-1702
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Carvalho Paulo S.¹^ORCID,Diniz Luan F.²,Ayala Alejandro P.³^ORCID

Affiliation:

1. Institute of Physics, Federal University of Mato Grosso do Sul, 79070-900, Campo Grande, MS, Brazil

2. Laboratório de Controle de Qualidade, Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901, Belo Horizonte, MG, Brazil

3. Departamento de Física, Universidade Federal do Ceará, 60455-970, Fortaleza, Ceará, Brazil

Abstract

Diastereomeric salts of (S,S)-sertraline, (Srt), with l- and d-tartaric acids have been prepared and their physical–chemical properties have been analyzed.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Alexander von Humboldt-Stiftung

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CE/D3CE00094J

Reference38 articles.

1. Crystallization of chiral molecular compounds: what can be learned from the Cambridge Structural Database?

2. Health Benefits and Pharmacological Properties of Carvone

3. The market of chiral drugs: Chiral switches versus de novo enantiomerically pure compounds

4. The predicated demise of racemic new molecular entities is an exaggeration

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