[CuBr(PPh3)3] for Azide−Alkyne Cycloaddition Reactions under Strict Click Conditions
Author:
Affiliation:
1. Department of Chemistry, Imperial College London, Exhibition Road, South Kensington, London SW7 2AZ, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo200085j
Reference49 articles.
1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions
2. Padwa, A.InComprehensive Organic Synthesis;Trost, B. M., Ed.Pergamon:Oxford, 1991; Vol.4, pp1069−1109.
3. Huisgen, R.In1,3-Dipolar Cycloaddition Chemistry;Padwa, A., Ed.Wiley:New York, 1984; pp1−176.
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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