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Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams

The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The utility of this reaction has been demonstrated in the synthesis of many natural products, materials, and pharmacological agents. In the last three decades, there has been a significant increase in the...

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Autor principal: Byrd, Katherine M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419509/
https://www.ncbi.nlm.nih.gov/pubmed/25977728
http://dx.doi.org/10.3762/bjoc.11.60
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author Byrd, Katherine M
author_facet Byrd, Katherine M
author_sort Byrd, Katherine M
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description The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The utility of this reaction has been demonstrated in the synthesis of many natural products, materials, and pharmacological agents. In the last three decades, there has been a significant increase in the development of asymmetric variants of this reaction. Unfortunately, conjugate addition reactions using α,β-unsaturated amides and lactams remain underdeveloped due to their inherently low reactivity. This review highlights the work that has been done on both diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams.
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spelling pubmed-44195092015-05-14 Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams Byrd, Katherine M Beilstein J Org Chem Review The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The utility of this reaction has been demonstrated in the synthesis of many natural products, materials, and pharmacological agents. In the last three decades, there has been a significant increase in the development of asymmetric variants of this reaction. Unfortunately, conjugate addition reactions using α,β-unsaturated amides and lactams remain underdeveloped due to their inherently low reactivity. This review highlights the work that has been done on both diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams. Beilstein-Institut 2015-04-23 /pmc/articles/PMC4419509/ /pubmed/25977728 http://dx.doi.org/10.3762/bjoc.11.60 Text en Copyright © 2015, Byrd https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Byrd, Katherine M
Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title_full Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title_fullStr Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title_full_unstemmed Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title_short Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
title_sort diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419509/
https://www.ncbi.nlm.nih.gov/pubmed/25977728
http://dx.doi.org/10.3762/bjoc.11.60
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