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Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations
The catalytic enantioselective ketimine Mannich and its related reactions provide direct access to chiral building blocks bearing an α-tertiary amine stereogenic center, a ubiquitous structural motif in nature. Although ketimines are often viewed as challenging electrophiles, various approaches/stra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570560/ https://www.ncbi.nlm.nih.gov/pubmed/34745653 http://dx.doi.org/10.3390/catal11060712 |
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author | Xu, Changgong Reep, Carlyn Jarvis, Jamielyn Naumann, Brandon Captain, Burjor Takenaka, Norito |
author_facet | Xu, Changgong Reep, Carlyn Jarvis, Jamielyn Naumann, Brandon Captain, Burjor Takenaka, Norito |
author_sort | Xu, Changgong |
collection | PubMed |
description | The catalytic enantioselective ketimine Mannich and its related reactions provide direct access to chiral building blocks bearing an α-tertiary amine stereogenic center, a ubiquitous structural motif in nature. Although ketimines are often viewed as challenging electrophiles, various approaches/strategies to circumvent or overcome the adverse properties of ketimines have been developed for these transformations. This review showcases the selected examples that highlight the benefits and utilities of various ketimines and remaining challenges associated with them in the context of Mannich, allylation, and aza-Morita-Baylis-Hillman reactions as well as their variants. |
format | Online Article Text |
id | pubmed-8570560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-85705602021-11-05 Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations Xu, Changgong Reep, Carlyn Jarvis, Jamielyn Naumann, Brandon Captain, Burjor Takenaka, Norito Catalysts Article The catalytic enantioselective ketimine Mannich and its related reactions provide direct access to chiral building blocks bearing an α-tertiary amine stereogenic center, a ubiquitous structural motif in nature. Although ketimines are often viewed as challenging electrophiles, various approaches/strategies to circumvent or overcome the adverse properties of ketimines have been developed for these transformations. This review showcases the selected examples that highlight the benefits and utilities of various ketimines and remaining challenges associated with them in the context of Mannich, allylation, and aza-Morita-Baylis-Hillman reactions as well as their variants. 2021-06-07 2021-06 /pmc/articles/PMC8570560/ /pubmed/34745653 http://dx.doi.org/10.3390/catal11060712 Text en https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Xu, Changgong Reep, Carlyn Jarvis, Jamielyn Naumann, Brandon Captain, Burjor Takenaka, Norito Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title | Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title_full | Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title_fullStr | Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title_full_unstemmed | Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title_short | Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations |
title_sort | asymmetric catalytic ketimine mannich reactions and related transformations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570560/ https://www.ncbi.nlm.nih.gov/pubmed/34745653 http://dx.doi.org/10.3390/catal11060712 |
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