A new synthetic pathway based on one-pot sequential aza-Michael addition and photoCuAAC click reactions-Reference-Cited by-同舟云学术

A new synthetic pathway based on one-pot sequential aza-Michael addition and photoCuAAC click reactions

Published:2019 Issue:9 Volume:9 Page:4824-4831
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Yin Boyang¹²³⁴,Croutxé-Barghorn Céline¹²³⁴^ORCID,Delaite Christelle¹²³⁴,Allonas Xavier¹²³⁴^ORCID

Affiliation:

1. Laboratory of Macromolecular Photochemistry and Engineering

2. University of Haute-Alsace

3. 68093 Mulhouse Cedex

4. France

Abstract

A solvent-free process is described for the synthesis of tailor-made molecules from a one-pot, two-step approach combining aza-Michael addition and photoinduced copper(i) catalysed azide–alkyne (photo-CuAAC) reactions.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C8RA10011J

Reference50 articles.

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

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

3. Synthesen in der hydroaromatischen Reihe

4. CANTHARIDIN. A STEREOSPECIFIC TOTAL SYNTHESIS

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