Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Philip, Rose Mary, Radhika, Sankaran, Saranya, P. V., Anilkumar, Gopinathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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
_version_ 1784698079973212160
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
work_keys_str_mv AT philiprosemary applicationsoftertbutanesulfinamideinthesynthesisofnheterocyclesviasulfinimines
AT radhikasankaran applicationsoftertbutanesulfinamideinthesynthesisofnheterocyclesviasulfinimines
AT saranyapv applicationsoftertbutanesulfinamideinthesynthesisofnheterocyclesviasulfinimines
AT anilkumargopinathan applicationsoftertbutanesulfinamideinthesynthesisofnheterocyclesviasulfinimines