A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines-Reference-Cited by-同舟云学术

A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines

Published:2020-06-05 Issue:24 Volume:2020 Page:3688-3698
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Silaichev Pavel S.¹²,Beryozkina Tetyana V.¹,Novikov Mikhail S.³,Dehaen Wim⁴^ORCID,Bakulev Vasiliy A.¹

Affiliation:

1. Ural Federal University named after the first President of Russia B. N. Yeltsin 19 Mira st. 620002 Yekaterinburg Russia

2. Department of Chemistry Perm State University 15 Bukireva st. 614990 Perm Russia

3. Institute of Chemistry St. Petersburg State University 7/9 Universitetskaya nab. 199034 St. Petersburg Russia

4. Molecular Design and Synthesis Department of Chemistry KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium

Funder

Russian Science Foundation

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202000453

Reference45 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. 1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview

4. Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles

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