Literature DB >> 16886066

Optical resolution methods.

Elemér Fogassy1, Mihály Nógrádi, Dávid Kozma, Gabriella Egri, Emese Pálovics, Violetta Kiss.   

Abstract

Despite the large number of elaborate enantioselective syntheses for the preparation of a single enantiomer to achieve industrial and scientific goals, the separation and purification of enantiomers (components of racemic compounds) is also necessary. Hence, we present the most often used thought-provoking modern methods based on momentous recognitions (e.g. spontaneous resolution, induced crystallization, resolution by formation of diastereomers, resolution by formation of non-covalent diastereomers, resolution by diastereomeric salt formation, resolution by diastereomeric complex formation, "half equivalent" methods of resolution, separation by crystallization, separation by distillation, separation by supercritical fluid extraction, resolution with mixtures of resolving agents, resolution with a derivative of the target compound, enantioselective chromatography, resolution by formation of covalent diastereomers, resolution by substrate selective reaction, kinetic resolution without enzymes, kinetic resolution by enzyme catalysis, hydrolytic and redox enzymes, kinetic and thermodynamic control, resolutions combined with 2nd order asymmetric transformations, enrichment of partially resolved mixtures, role of the solvent and methods of optimization in the separation of diastereoisomers, non-linear effects and selected examples of resolution on an industrial scale).

Year:  2006        PMID: 16886066     DOI: 10.1039/b603058k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  12 in total

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Journal:  ACS Med Chem Lett       Date:  2021-07-16       Impact factor: 4.632

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Authors:  Ernlie A Publicover; Jennifer Kolwich; Darcie L Stack; Alyssa J Doué; Kai E O Ylijoki
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2017-04-18

4.  Syntheses, Characterization, Resolution, and Biological Studies of Coordination Compounds of Aspartic Acid and Glycine.

Authors:  Temitayo Aiyelabola; Ezekiel Akinkunmi; Isaac Ojo; Efere Obuotor; Clement Adebajo; David Isabirye
Journal:  Bioinorg Chem Appl       Date:  2017-02-15       Impact factor: 7.778

5.  A Gallium-based Chiral Solvating Agent Enables the Use of 1H NMR Spectroscopy to Differentiate Chiral Alcohols.

Authors:  Sumin Jang; Hyunwoo Kim
Journal:  iScience       Date:  2019-08-02

6.  Crystallization-Induced Deracemization: Experiments and Modeling.

Authors:  Brigitta Bodák; Francesca Breveglieri; Marco Mazzotti
Journal:  Cryst Growth Des       Date:  2022-01-06       Impact factor: 4.076

7.  Enzymatic Approach to the Synthesis of Enantiomerically Pure Hydroxy Derivatives of 1,3,5-Triaza-7-phosphaadamantane.

Authors:  Małgorzata Kwiatkowska; Jarosław Błaszczyk; Lesław Sieroń; Piotr Kiełbasiński
Journal:  J Org Chem       Date:  2021-06-17       Impact factor: 4.354

8.  Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.

Authors:  William L Scott; Jordi Alsina; Christopher O Audu; Evgenii Babaev; Linda Cook; Jeffery L Dage; Lawrence A Goodwin; Jacek G Martynow; Dariusz Matosiuk; Miriam Royo; Judith G Smith; Andrew T Strong; Kirk Wickizer; Eric M Woerly; Ziniu Zhou; Martin J O'Donnell
Journal:  J Comb Chem       Date:  2009 Jan-Feb

9.  Highly efficient enantioselective liquid-liquid extraction of 1,2-amino-alcohols using SPINOL based phosphoric acid hosts.

Authors:  Erik B Pinxterhuis; Jean-Baptiste Gualtierotti; Hero J Heeres; Johannes G de Vries; Ben L Feringa
Journal:  Chem Sci       Date:  2017-07-21       Impact factor: 9.825

10.  Role of Additives during Deracemization Using Temperature Cycling.

Authors:  Giuseppe Belletti; Hugo Meekes; Floris P J T Rutjes; Elias Vlieg
Journal:  Cryst Growth Des       Date:  2018-10-02       Impact factor: 4.076

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