Triazolated calix[4]arenes from 2-azidoethylated precursors: is there a difference in the way the triazoles are attached to narrow rims?-Reference-Cited by-同舟云学术

Triazolated calix[4]arenes from 2-azidoethylated precursors: is there a difference in the way the triazoles are attached to narrow rims?

Published:2019 Issue:11 Volume:43 Page:4562-4580
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Gorbunov Alexander¹²³⁴^ORCID,Kuznetsova Julia¹²³⁴,Puchnin Kirill¹²³⁴^ORCID,Kovalev Vladimir¹²³⁴^ORCID,Vatsouro Ivan¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. M. V. Lomonosov Moscow State University

3. 119991 Moscow

4. Russia

Abstract

A large series of narrow-rim 4-R-1-triazolated calix[4]arenes was prepared, and these compounds were compared in terms of their cation-binding ability with the ‘inverted’ 1-R-4-triazolated calix[4]arenes.

Funder

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ06464D

Reference82 articles.

1. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

3. Cu-Catalyzed Azide−Alkyne Cycloaddition

4. Triazole: a unique building block for the construction of functional materials

5. The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview

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