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Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines
Chiral sulfinamides are among the best known chiral auxiliaries in the stereoselective synthesis of amines and their derivatives. The most extensively used enantiopure tert-butanesulfinamide emerged as the gold standard among many others over the last two decades. The present review attempts to prov...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058287/ https://www.ncbi.nlm.nih.gov/pubmed/35516764 http://dx.doi.org/10.1039/d0ra08819f |
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author | Philip, Rose Mary Radhika, Sankaran Saranya, P. V. Anilkumar, Gopinathan |
author_facet | Philip, Rose Mary Radhika, Sankaran Saranya, P. V. Anilkumar, Gopinathan |
author_sort | Philip, Rose Mary |
collection | PubMed |
description | Chiral sulfinamides are among the best known chiral auxiliaries in the stereoselective synthesis of amines and their derivatives. The most extensively used enantiopure tert-butanesulfinamide emerged as the gold standard among many others over the last two decades. The present review attempts to provide an overview of tert-butanesulfinamide mediated asymmetric N-heterocycle synthesis via sulfinimines and covers literature from 2010–2020. This methodology offers general access to structurally diverse piperidines, pyrrolidines, azetidines, and their fused derivatives that represent the structural motif of many natural products and therapeutically applicable compounds. |
format | Online Article Text |
id | pubmed-9058287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90582872022-05-04 Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines Philip, Rose Mary Radhika, Sankaran Saranya, P. V. Anilkumar, Gopinathan RSC Adv Chemistry Chiral sulfinamides are among the best known chiral auxiliaries in the stereoselective synthesis of amines and their derivatives. The most extensively used enantiopure tert-butanesulfinamide emerged as the gold standard among many others over the last two decades. The present review attempts to provide an overview of tert-butanesulfinamide mediated asymmetric N-heterocycle synthesis via sulfinimines and covers literature from 2010–2020. This methodology offers general access to structurally diverse piperidines, pyrrolidines, azetidines, and their fused derivatives that represent the structural motif of many natural products and therapeutically applicable compounds. The Royal Society of Chemistry 2020-11-23 /pmc/articles/PMC9058287/ /pubmed/35516764 http://dx.doi.org/10.1039/d0ra08819f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Philip, Rose Mary Radhika, Sankaran Saranya, P. V. Anilkumar, Gopinathan Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title | Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title_full | Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title_fullStr | Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title_full_unstemmed | Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title_short | Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines |
title_sort | applications of tert-butanesulfinamide in the synthesis of n-heterocycles via sulfinimines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058287/ https://www.ncbi.nlm.nih.gov/pubmed/35516764 http://dx.doi.org/10.1039/d0ra08819f |
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