Absolute configuration and crystal packing for three chiral drugs prone to spontaneous resolution: Guaifenesin, methocarbamol and mephenesin-Reference-Cited by-同舟云学术

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Absolute configuration and crystal packing for three chiral drugs prone to spontaneous resolution: Guaifenesin, methocarbamol and mephenesin

Published:2009-02 Issue:1-3 Volume:920 Page:377-382
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Bredikhin Alexander A.,Gubaidullin Aidar T.,Bredikhina Zemfira A.,Krivolapov Dmitry B.,Pashagin Alexander V.,Litvinov Igor A.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference22 articles.

1. Chiral Discrimination during Crystallization

2. Optical resolution methods

3. Chiral Discrimination in Low-Density Hydrogen-Bonded Frameworks

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discovery, Characterization, and Solid-State Quantification of the Racemic Compound of Guaifenesin;Crystal Growth & Design;2024-05-31

2. Chemoenzymatic Synthesis of Chiral Building Blocks Based on the Kinetic Resolution of Glycerol‐Derived Cyclic Carbonates;ChemCatChem;2023-08-30

3. Multivariate Analysis of a Highly Effective Drug Combination Tablet Containing the Antiepileptic Drug Gabapentin to Enhance Pharmaceutical Properties with a Multicomponent Crystal Strategy;Crystal Growth & Design;2022-11-07

4. Identifying a Hidden Conglomerate Chiral Pool in the CSD;JACS Au;2022-09-23

5. Crystal Landscape of Chiral Drug Chlorphenesin and Its Structural Analogues: Polymorphism of Racemic and Enantiopure Samples, Metastable and Stable Racemic Conglomerates, Diverse in Unity Crystal Motifs;Crystal Growth & Design;2021-05-20

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