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Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams
Benzo-fused γ-lactam rings such as isoindolin-2-ones and 2-oxindoles are part of the structure of many pharmaceutically active molecules. They can be often synthesized by means of multicomponent approaches and recent contributions in this field are summarized in this review. Clear advantages of thes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541321/ https://www.ncbi.nlm.nih.gov/pubmed/31164944 http://dx.doi.org/10.3762/bjoc.15.104 |
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author | de Marigorta, Edorta Martínez Santos, Jesús M de Los Ochoa de Retana, Ana M Vicario, Javier Palacios, Francisco |
author_facet | de Marigorta, Edorta Martínez Santos, Jesús M de Los Ochoa de Retana, Ana M Vicario, Javier Palacios, Francisco |
author_sort | de Marigorta, Edorta Martínez |
collection | PubMed |
description | Benzo-fused γ-lactam rings such as isoindolin-2-ones and 2-oxindoles are part of the structure of many pharmaceutically active molecules. They can be often synthesized by means of multicomponent approaches and recent contributions in this field are summarized in this review. Clear advantages of these methods include the efficiency in saving raw materials and working time. However, there is still a need of new catalytic systems to allow the enantioselective preparation of these heterocycles by multicomponent reactions. |
format | Online Article Text |
id | pubmed-6541321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-65413212019-06-04 Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams de Marigorta, Edorta Martínez Santos, Jesús M de Los Ochoa de Retana, Ana M Vicario, Javier Palacios, Francisco Beilstein J Org Chem Review Benzo-fused γ-lactam rings such as isoindolin-2-ones and 2-oxindoles are part of the structure of many pharmaceutically active molecules. They can be often synthesized by means of multicomponent approaches and recent contributions in this field are summarized in this review. Clear advantages of these methods include the efficiency in saving raw materials and working time. However, there is still a need of new catalytic systems to allow the enantioselective preparation of these heterocycles by multicomponent reactions. Beilstein-Institut 2019-05-08 /pmc/articles/PMC6541321/ /pubmed/31164944 http://dx.doi.org/10.3762/bjoc.15.104 Text en Copyright © 2019, de Marigorta et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review de Marigorta, Edorta Martínez Santos, Jesús M de Los Ochoa de Retana, Ana M Vicario, Javier Palacios, Francisco Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title | Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title_full | Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title_fullStr | Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title_full_unstemmed | Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title_short | Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams |
title_sort | multicomponent reactions (mcrs): a useful access to the synthesis of benzo-fused γ-lactams |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541321/ https://www.ncbi.nlm.nih.gov/pubmed/31164944 http://dx.doi.org/10.3762/bjoc.15.104 |
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