General Method for the Synthesis of 1,4-Disubstituted 5-Halo-1,2,3-triazoles-Reference-Cited by-同舟云学术

General Method for the Synthesis of 1,4-Disubstituted 5-Halo-1,2,3-triazoles

Published:2017-09-19 Issue:35 Volume:2017 Page:5225-5230
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Gribanov Pavel S.¹,Topchiy Maxim A.¹,Karsakova Iuliia V.²,Chesnokov Gleb A.²,Smirnov Alexander Yu.¹,Minaeva Lidiya I.³,Asachenko Andrey F.¹³,Nechaev Mikhail S.¹²^ORCID

Affiliation:

1. A. V. Topchiev Institute of Petrochemical Synthesis; Russian Academy of Sciences; Lenynsky Prospect 29 119991 Moscow Russian Federation

2. M. V. Lomonosov Moscow State University; Leninskie Gory 1 (3) 119991 Moscow Russian Federation

3. Peoples' Friendship University of Russia; Miklukho-Maklay St., 6 117198 Moscow Russian Federation

Funder

Russian Science Foundation

Ministry of Education and Science of the Russian Federation

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference55 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. Recent advances in the Cu(i)-catalyzed azide–alkyne cycloaddition: focus on functionally substituted azides and alkynes

4. Click chemistry: function follows form

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