Iodide ion-enabled highly regioselective α-C(sp<sup>3</sup>)–H triazolization of ethers with <i>N</i>-sulfonyl-1,2,3-triazoles-Reference-Cited by-同舟云学术

Iodide ion-enabled highly regioselective α-C(sp³)–H triazolization of ethers with N-sulfonyl-1,2,3-triazoles

Published:2024 Issue:34 Volume:48 Page:15002-15007
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Deng Yaqi¹,Yin Jiabin¹,Hu Zongjing¹,Xue Jian¹,Ji Jian¹,Zhu Tong¹^ORCID,Liu Shunying¹^ORCID

Affiliation:

1. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China

Abstract

A highly regioselective construction of N2-substituted hemiaminal ethers was established via a synergetic SN2-like radical coupling mechanism.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ02699C

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