Enantioconvergent catalysis

An enantioconvergent catalytic process has the potential to convert a racemic starting material to a single highly enantioenriched product with a maximum yield of 100%. Three mechanistically distinct approaches to effecting enantioconvergent catalysis are identified, and recent examples of each are...

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Main Authors: Justin T. Mohr, Jared T. Moore, Brian M. Stoltz
Format: Article
Language:English
Published: Beilstein-Institut 2016-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.12.192
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author Justin T. Mohr
Jared T. Moore
Brian M. Stoltz
author_facet Justin T. Mohr
Jared T. Moore
Brian M. Stoltz
author_sort Justin T. Mohr
collection DOAJ
description An enantioconvergent catalytic process has the potential to convert a racemic starting material to a single highly enantioenriched product with a maximum yield of 100%. Three mechanistically distinct approaches to effecting enantioconvergent catalysis are identified, and recent examples of each are highlighted. These processes are compared to related, non-enantioconvergent methods.
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spelling doaj.art-05f0fbec54bf4cceb0823eeed12f3fc62022-12-21T22:47:13ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972016-09-011212038204510.3762/bjoc.12.1921860-5397-12-192Enantioconvergent catalysisJustin T. Mohr0Jared T. Moore1Brian M. Stoltz2Department of Chemistry, University of Illinois at Chicago, 845 West Taylor St., Chicago, IL 60607, USAThe Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering California Institute of Technology, 1200 E California Blvd. MC 101-20, Pasadena, CA 91125, USA, Fax: (+1) 626-395-8436The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering California Institute of Technology, 1200 E California Blvd. MC 101-20, Pasadena, CA 91125, USA, Fax: (+1) 626-395-8436An enantioconvergent catalytic process has the potential to convert a racemic starting material to a single highly enantioenriched product with a maximum yield of 100%. Three mechanistically distinct approaches to effecting enantioconvergent catalysis are identified, and recent examples of each are highlighted. These processes are compared to related, non-enantioconvergent methods.https://doi.org/10.3762/bjoc.12.192asymmetric catalysisenantioselectivitysynthetic methods
spellingShingle Justin T. Mohr
Jared T. Moore
Brian M. Stoltz
Enantioconvergent catalysis
Beilstein Journal of Organic Chemistry
asymmetric catalysis
enantioselectivity
synthetic methods
title Enantioconvergent catalysis
title_full Enantioconvergent catalysis
title_fullStr Enantioconvergent catalysis
title_full_unstemmed Enantioconvergent catalysis
title_short Enantioconvergent catalysis
title_sort enantioconvergent catalysis
topic asymmetric catalysis
enantioselectivity
synthetic methods
url https://doi.org/10.3762/bjoc.12.192
work_keys_str_mv AT justintmohr enantioconvergentcatalysis
AT jaredtmoore enantioconvergentcatalysis
AT brianmstoltz enantioconvergentcatalysis