The enantiopreference in the solid state probed in lamivudine crystal forms with mandelic acid-Reference-Cited by-同舟云学术

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The enantiopreference in the solid state probed in lamivudine crystal forms with mandelic acid

Published:2015 Issue:26 Volume:5 Page:20486-20490
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

da Silva Cameron Capeletti¹²³⁴,Martins Felipe Terra¹²³⁴

Affiliation:

1. Instituto de Química

2. Universidade Federal de Goiás

3. Goiânia

4. Brazil

Abstract

Chiral recognition, even when there is not chiral resolution, observed in two crystal forms of lamivudine with mandelic acid.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA01398D

Reference27 articles.

1. Spontaneous racemic resolution – towards control of molecular recognition nature

2. Resolution of sertraline with (R)-mandelic acid: Chiral discrimination mechanism study

3. Chirality Switching in Optical Resolution of Mandelic Acid in C1–C4 Alcohols: Elucidation of Solvent Effects Based on X-ray Crystal Structures of Diastereomeric Salts

4. Innovative Chiral Resolution Using Enantiospecific Co-Crystallization in Solution

5. Cocrystal Formation between Chiral Compounds: How Cocrystals Differ from Salts

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1. Ligand-Receptor Interactions of Lamivudine: A View from Charge Density Study and QM/MM Calculations;Biomedicines;2023-03-01

2. Strategies for chiral separation: from racemate to enantiomer;Chemical Science;2023

3. Co-crystals of zwitterionic GABA API's pregabalin and phenibut: properties and application;CrystEngComm;2022

4. Chirality and stereoisomerism of organic multicomponent crystals in the CSD;CrystEngComm;2020

5. Structural Analysis of d-Phenylglycinamide Salts Uncovers Potential Pitfalls in Chiral Resolution via Diastereomeric Salt Formation;Crystal Growth & Design;2019-06-10

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