Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives

Chiral and hindered triazolopyridinone derivatives are an underexplored area of chemical space mainly due to their challenging synthesis via classical methods. Here, the authors report an electrochemical rearrangement for the synthesis of triazolopyridinones using diverse, available alkyl carboxylic...

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Autores principales:	Zenghui Ye, Yanqi Wu, Na Chen, Hong Zhang, Kai Zhu, Mingruo Ding, Min Liu, Yong Li, Fengzhi Zhang
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2020
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/738cfb6b38a84e0f990f74d1bfe7f678
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spelling	oai:doaj.org-article:738cfb6b38a84e0f990f74d1bfe7f6782021-12-02T16:26:25ZEnantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives10.1038/s41467-020-17389-w2041-1723https://doaj.org/article/738cfb6b38a84e0f990f74d1bfe7f6782020-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-17389-whttps://doaj.org/toc/2041-1723Chiral and hindered triazolopyridinone derivatives are an underexplored area of chemical space mainly due to their challenging synthesis via classical methods. Here, the authors report an electrochemical rearrangement for the synthesis of triazolopyridinones using diverse, available alkyl carboxylic acids as starting materials.Zenghui YeYanqi WuNa ChenHong ZhangKai ZhuMingruo DingMin LiuYong LiFengzhi ZhangNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Zenghui Ye Yanqi Wu Na Chen Hong Zhang Kai Zhu Mingruo Ding Min Liu Yong Li Fengzhi Zhang Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
description	Chiral and hindered triazolopyridinone derivatives are an underexplored area of chemical space mainly due to their challenging synthesis via classical methods. Here, the authors report an electrochemical rearrangement for the synthesis of triazolopyridinones using diverse, available alkyl carboxylic acids as starting materials.
format	article
author	Zenghui Ye Yanqi Wu Na Chen Hong Zhang Kai Zhu Mingruo Ding Min Liu Yong Li Fengzhi Zhang
author_facet	Zenghui Ye Yanqi Wu Na Chen Hong Zhang Kai Zhu Mingruo Ding Min Liu Yong Li Fengzhi Zhang
author_sort	Zenghui Ye
title	Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
title_short	Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
title_full	Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
title_fullStr	Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
title_full_unstemmed	Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
title_sort	enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives
publisher	Nature Portfolio
publishDate	2020
url	https://doaj.org/article/738cfb6b38a84e0f990f74d1bfe7f678
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Enantiospecific electrochemical rearrangement for the synthesis of hindered triazolopyridinone derivatives

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