Promotion of 1,3-dipolar cycloaddition between azides and β-enaminones by deep eutectic solvents-Reference-Cited by-同舟云学术

Promotion of 1,3-dipolar cycloaddition between azides and β-enaminones by deep eutectic solvents

Published:2016 Issue:7 Volume:40 Page:5989-5992
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Martins Marcos Antonio Pinto¹²³⁴⁵,Paveglio Guilherme Caneppele¹²³⁴⁵,Rodrigues Leticia Valvassori¹²³⁴⁵,Frizzo Clarissa Piccinin¹²³⁴⁵,Zanatta Nilo¹²³⁴⁵,Bonacorso Helio Gauze¹²³⁴⁵

Affiliation:

1. Núcleo de Química de Heterociclos (NUQUIMHE)

2. Departamento de Química

3. Universidade Federal de Santa Maria

4. 97105-900 Santa Maria

5. Brazil

Abstract

The metal-free, high selectivity and efficient synthesis of 4-acyl triazoles in a DES (ChCl:ethylene glycol) is reported.

Funder

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/NJ/C5NJ03654B

Reference32 articles.

1. R. Huisgen , Proceedings of the Chemical Society, London, 1961, p. 357

2. 1,3-Dipolar Cycloaddition Chemistry, ed. R. Huisgen and A. Pawda, Wiley, New York, 1984, p. 1

3. Kinetics and reaction mechanisms: selected examples from the experience of forty years

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

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

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