Alkynyl‐ or Azido‐Functionalized 1,2,3‐Triazoles: Selective MonoCuAAC Promoted by Physical Factors-Reference-Cited by-同舟云学术

Alkynyl‐ or Azido‐Functionalized 1,2,3‐Triazoles: Selective MonoCuAAC Promoted by Physical Factors

Published:2019-07 Issue:25 Volume:4 Page:7470-7475
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Topchiy Maxim A.¹²,Ageshina Alexandra A.¹,Chesnokov Gleb A.¹,Sterligov Grigorii K.¹²,Rzhevskiy Sergey A.¹,Gribanov Pavel S.¹³,Osipov Sergey N.³,Nechaev Mikhail S.¹²,Asachenko Andrey F.¹²^ORCID

Affiliation:

1. A. V. Topchiev Institute of Petrochemical SynthesisRussian Academy of Sciences 29 Leninsky Prospect 119991 Moscow Russian Federation

2. Department of ChemistryM. V. Lomonosov Moscow State University, 1/3 Leninskie gory 119991 Moscow Russian Federation

3. A. N. Nesmeyanov Institute of Organoelement CompoundsRussian Academy of Sciences 28 Vavilov str. 119991 Moscow Russian Federation

Funder

Russian Science Foundation

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201902135

Reference108 articles.

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

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

4. Advances of azide-alkyne cycloaddition-click chemistry over the recent decade

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