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Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents

[Image: see text] A novel, efficient, and simple method for the resolution of racemic mixtures is presented in which PEGylated resolving agents are subjected to diastereomeric complex formation in alcohols. The resulting complexes then undergo temperature-assisted phase transition, affording a preci...

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Autores principales: Mokhtari, Javad, Azarnoosh, Sahar, Karimian, Khashayar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645586/
https://www.ncbi.nlm.nih.gov/pubmed/31457403
http://dx.doi.org/10.1021/acsomega.7b01070
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author Mokhtari, Javad
Azarnoosh, Sahar
Karimian, Khashayar
author_facet Mokhtari, Javad
Azarnoosh, Sahar
Karimian, Khashayar
author_sort Mokhtari, Javad
collection PubMed
description [Image: see text] A novel, efficient, and simple method for the resolution of racemic mixtures is presented in which PEGylated resolving agents are subjected to diastereomeric complex formation in alcohols. The resulting complexes then undergo temperature-assisted phase transition, affording a precipitate that is enriched in one enantiomer and separable by filtration. In an aqueous solution, phase transition can be caused by the methods used in the precipitation of poly(ethylene glycol) (e.g., addition of ammonium sulfate). A number of racemic amines have been successfully resolved using this method. The first cycle of resolution affords the amines with an optical purity of 72–85% from their corresponding racemic mixture in good yields (78–90%). An additional cycle improved the optical purity to 87–95%. The PEGylated resolving agents can be recovered and reutilized without the loss of resolution efficiency.
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spelling pubmed-66455862019-08-27 Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents Mokhtari, Javad Azarnoosh, Sahar Karimian, Khashayar ACS Omega [Image: see text] A novel, efficient, and simple method for the resolution of racemic mixtures is presented in which PEGylated resolving agents are subjected to diastereomeric complex formation in alcohols. The resulting complexes then undergo temperature-assisted phase transition, affording a precipitate that is enriched in one enantiomer and separable by filtration. In an aqueous solution, phase transition can be caused by the methods used in the precipitation of poly(ethylene glycol) (e.g., addition of ammonium sulfate). A number of racemic amines have been successfully resolved using this method. The first cycle of resolution affords the amines with an optical purity of 72–85% from their corresponding racemic mixture in good yields (78–90%). An additional cycle improved the optical purity to 87–95%. The PEGylated resolving agents can be recovered and reutilized without the loss of resolution efficiency. American Chemical Society 2017-12-07 /pmc/articles/PMC6645586/ /pubmed/31457403 http://dx.doi.org/10.1021/acsomega.7b01070 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Mokhtari, Javad
Azarnoosh, Sahar
Karimian, Khashayar
Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title_full Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title_fullStr Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title_full_unstemmed Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title_short Resolution of Racemic Mixtures by Phase Transition of PEGylated Resolving Agents
title_sort resolution of racemic mixtures by phase transition of pegylated resolving agents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645586/
https://www.ncbi.nlm.nih.gov/pubmed/31457403
http://dx.doi.org/10.1021/acsomega.7b01070
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