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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2015
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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 |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-4419509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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