Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles-Reference-Cited by-同舟云学术

Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles

Published:2019 Issue:15 Volume:21 Page:4211-4216
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhang Dongsheng¹²³⁴,Fan Yingzhu¹²³⁴,Yan Zhongliang¹²³⁴,Nie Yi¹²³⁴,Xiong Xingquan¹²³⁴^ORCID,Gao Lizhu¹²³⁴^ORCID

Affiliation:

1. College of Materials Science & Engineering

2. Huaqiao University

3. Xiamen

4. China

Abstract

A metal-free route to 1,4-disubstituted and 1,4,5-trisubstituted formyl triazoles was developed. One 1,2,3-triazole containing diastereotopic protons was identified.

Funder

Huaqiao University

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/GC/C9GC01129C

Reference103 articles.

1. Medicinal attributes of 1,2,3-triazoles: Current developments

2. Click Chemistry for Drug Development and Diverse Chemical–Biology Applications

3. 1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

4. Click Chemistry Finds Its Way into Covalent Porous Organic Materials

5. Click-chemistry approaches to π-conjugated polymers for organic electronics applications

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