Cargando…

Light-induced metal-free transformations of unactivated pyridotriazoles

A highly efficient and practical method for incorporation of the arylmethylpyridyl moiety into diverse molecules has been developed. This method features the transition metal-free light-induced room temperature transformation of pyridotriazoles into pyridyl carbenes, which are capable of smooth aryl...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Ziyan, Yadagiri, Dongari, Gevorgyan, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844233/
https://www.ncbi.nlm.nih.gov/pubmed/31803418
http://dx.doi.org/10.1039/c9sc02448d
_version_ 1783468395936612352
author Zhang, Ziyan
Yadagiri, Dongari
Gevorgyan, Vladimir
author_facet Zhang, Ziyan
Yadagiri, Dongari
Gevorgyan, Vladimir
author_sort Zhang, Ziyan
collection PubMed
description A highly efficient and practical method for incorporation of the arylmethylpyridyl moiety into diverse molecules has been developed. This method features the transition metal-free light-induced room temperature transformation of pyridotriazoles into pyridyl carbenes, which are capable of smooth arylation, X–H insertion, and cyclopropanation reactions. The synthetic usefulness of the developed method was illustrated in a facile synthesis of biologically active molecules.
format Online
Article
Text
id pubmed-6844233
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-68442332019-12-04 Light-induced metal-free transformations of unactivated pyridotriazoles Zhang, Ziyan Yadagiri, Dongari Gevorgyan, Vladimir Chem Sci Chemistry A highly efficient and practical method for incorporation of the arylmethylpyridyl moiety into diverse molecules has been developed. This method features the transition metal-free light-induced room temperature transformation of pyridotriazoles into pyridyl carbenes, which are capable of smooth arylation, X–H insertion, and cyclopropanation reactions. The synthetic usefulness of the developed method was illustrated in a facile synthesis of biologically active molecules. Royal Society of Chemistry 2019-07-25 /pmc/articles/PMC6844233/ /pubmed/31803418 http://dx.doi.org/10.1039/c9sc02448d Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Zhang, Ziyan
Yadagiri, Dongari
Gevorgyan, Vladimir
Light-induced metal-free transformations of unactivated pyridotriazoles
title Light-induced metal-free transformations of unactivated pyridotriazoles
title_full Light-induced metal-free transformations of unactivated pyridotriazoles
title_fullStr Light-induced metal-free transformations of unactivated pyridotriazoles
title_full_unstemmed Light-induced metal-free transformations of unactivated pyridotriazoles
title_short Light-induced metal-free transformations of unactivated pyridotriazoles
title_sort light-induced metal-free transformations of unactivated pyridotriazoles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844233/
https://www.ncbi.nlm.nih.gov/pubmed/31803418
http://dx.doi.org/10.1039/c9sc02448d
work_keys_str_mv AT zhangziyan lightinducedmetalfreetransformationsofunactivatedpyridotriazoles
AT yadagiridongari lightinducedmetalfreetransformationsofunactivatedpyridotriazoles
AT gevorgyanvladimir lightinducedmetalfreetransformationsofunactivatedpyridotriazoles