A mild protocol for efficient preparation of functional molecules containing triazole-Reference-Cited by-同舟云学术

A mild protocol for efficient preparation of functional molecules containing triazole

Published:2024 Issue:11 Volume:14 Page:7601-7608
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Leng Jing¹^ORCID,Xu Jie¹,Li Yanan¹,Wang Shi-Meng²,Qin Hua-Li³^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Yangzhou Polytechnic Institute, Yangzhou, Jiangsu 225127, P. R. China

2. Xiangyang Public Inspection and Testing Center, No. 69, Taiziwan Road, Xiangyang, Hubei Province 441000, P. R. China

3. State Key Laboratory of Silicate Materials for Architectures, School of Chemistry, Chemical Engineering and Life Science, Wuhan University of Technology, 205 Luoshi Road, Wuhan, Hubei Province, 430070, P. R. China

Abstract

Novel triazole molecules containing sulfonyl fluoride functionalities were achieved through Cu-catalyzed click chemistry, and the sulfonyl fluoride moieties were cleaved under base conditions to produce N-unsubstituted triazoles quantitatively.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D4RA01271B

Reference53 articles.

1. 4-Aryl-1,2,3-triazole: A Novel Template for a Reversible Methionine Aminopeptidase 2 Inhibitor, Optimized To Inhibit Angiogenesis in Vivo

2. Synthesis and Antiprotozoal Activity of Cationic 1,4-Diphenyl-1H-1,2,3-triazoles

3. 1,2,3-Triazole-Functionalized Polysulfone Synthesis through Microwave-Assisted Copper-Catalyzed Click Chemistry: A Highly Proton Conducting High Temperature Membrane

4. Reversible CO Scavenging via Adsorbate-Dependent Spin State Transitions in an Iron(II)–Triazolate Metal–Organic Framework

5. Click Chemistry: Diverse Chemical Function from a Few Good Reactions