Cargando…

Salient features of the aza-Wacker cyclization reaction

The intramolecular aza-Wacker reaction has unparalleled potential for the site-selective amination of olefins, but it is perhaps underappreciated relative to other alkene oxidations. The first part of this review makes the distinction between classical and tethered aza-Wacker cyclization reactions a...

Descripción completa

Detalles Bibliográficos
Autores principales: Thomas, Annu Anna, Nagamalla, Someshwar, Sathyamoorthi, Shyam
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/PMC8163389/
https://www.ncbi.nlm.nih.gov/pubmed/34123081
http://dx.doi.org/10.1039/d0sc02554b
_version_ 1783700903409221632
author Thomas, Annu Anna
Nagamalla, Someshwar
Sathyamoorthi, Shyam
author_facet Thomas, Annu Anna
Nagamalla, Someshwar
Sathyamoorthi, Shyam
author_sort Thomas, Annu Anna
collection PubMed
description The intramolecular aza-Wacker reaction has unparalleled potential for the site-selective amination of olefins, but it is perhaps underappreciated relative to other alkene oxidations. The first part of this review makes the distinction between classical and tethered aza-Wacker cyclization reactions and summarizes examples of the latter. The second portion focuses on developments in asymmetric aza-Wacker cyclization technology. The final part of the review summarizes applications of all classes of aza-Wacker cyclization reactions to natural product assembly.
format Online
Article
Text
id pubmed-8163389
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-81633892021-06-11 Salient features of the aza-Wacker cyclization reaction Thomas, Annu Anna Nagamalla, Someshwar Sathyamoorthi, Shyam Chem Sci Chemistry The intramolecular aza-Wacker reaction has unparalleled potential for the site-selective amination of olefins, but it is perhaps underappreciated relative to other alkene oxidations. The first part of this review makes the distinction between classical and tethered aza-Wacker cyclization reactions and summarizes examples of the latter. The second portion focuses on developments in asymmetric aza-Wacker cyclization technology. The final part of the review summarizes applications of all classes of aza-Wacker cyclization reactions to natural product assembly. The Royal Society of Chemistry 2020-07-21 /pmc/articles/PMC8163389/ /pubmed/34123081 http://dx.doi.org/10.1039/d0sc02554b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Thomas, Annu Anna
Nagamalla, Someshwar
Sathyamoorthi, Shyam
Salient features of the aza-Wacker cyclization reaction
title Salient features of the aza-Wacker cyclization reaction
title_full Salient features of the aza-Wacker cyclization reaction
title_fullStr Salient features of the aza-Wacker cyclization reaction
title_full_unstemmed Salient features of the aza-Wacker cyclization reaction
title_short Salient features of the aza-Wacker cyclization reaction
title_sort salient features of the aza-wacker cyclization reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163389/
https://www.ncbi.nlm.nih.gov/pubmed/34123081
http://dx.doi.org/10.1039/d0sc02554b
work_keys_str_mv AT thomasannuanna salientfeaturesoftheazawackercyclizationreaction
AT nagamallasomeshwar salientfeaturesoftheazawackercyclizationreaction
AT sathyamoorthishyam salientfeaturesoftheazawackercyclizationreaction