Cargando…

Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines

This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxindoles based on enantioselective catalytic nucleophilic additions to isatin imines published since the beginning of 2015.

Detalles Bibliográficos
Autor principal: Pellissier, Hélène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009130/
https://www.ncbi.nlm.nih.gov/pubmed/29977400
http://dx.doi.org/10.3762/bjoc.14.114
_version_ 1783333315103686656
author Pellissier, Hélène
author_facet Pellissier, Hélène
author_sort Pellissier, Hélène
collection PubMed
description This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxindoles based on enantioselective catalytic nucleophilic additions to isatin imines published since the beginning of 2015.
format Online
Article
Text
id pubmed-6009130
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-60091302018-07-05 Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines Pellissier, Hélène Beilstein J Org Chem Review This review collects the recent developments in the synthesis of chiral 3-substituted 3-amino-2-oxindoles based on enantioselective catalytic nucleophilic additions to isatin imines published since the beginning of 2015. Beilstein-Institut 2018-06-06 /pmc/articles/PMC6009130/ /pubmed/29977400 http://dx.doi.org/10.3762/bjoc.14.114 Text en Copyright © 2018, Pellissier 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), 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
Pellissier, Hélène
Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title_full Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title_fullStr Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title_full_unstemmed Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title_short Synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
title_sort synthesis of chiral 3-substituted 3-amino-2-oxindoles through enantioselective catalytic nucleophilic additions to isatin imines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009130/
https://www.ncbi.nlm.nih.gov/pubmed/29977400
http://dx.doi.org/10.3762/bjoc.14.114
work_keys_str_mv AT pellissierhelene synthesisofchiral3substituted3amino2oxindolesthroughenantioselectivecatalyticnucleophilicadditionstoisatinimines