Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry-Reference-Cited by-同舟云学术

Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry

Published:2017 Issue:6 Volume:4 Page:978-985
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Morozova Maria A.¹²³⁴,Yusubov Mekhman S.⁵²³⁴,Kratochvil Bohumil⁶²³⁴⁷,Eigner Václav⁷⁸⁹¹⁰,Bondarev Alexander A.¹¹¹²¹³⁴,Yoshimura Akira⁵²³⁴¹⁴,Saito Akio¹⁵¹⁶¹⁷^ORCID,Zhdankin Viktor V.⁵²³⁴¹⁴,Trusova Marina E.¹²³⁴,Postnikov Pavel S.⁵²³⁴^ORCID

Affiliation:

1. Department of Biotechnology and Organic Chemistry

2. National Research Tomsk Polytechnic University

3. 634050 Tomsk

4. Russia

5. Department of Technology of Organic Substances and Polymer Materials

6. Department of Physical and Analytical Chemistry

7. Department of Solid State Chemistry

8. University of Chemistry and Technology

9. Prague, Technicka 5

10. Czech Republic

11. Department of Biomedicine

12. Altai State University

13. Barnaul, Lenina av. 61

14. Department of Chemistry and Biochemistry

15. Division of Applied Chemistry Institute of Engineering Tokyo University of Agriculture and Technology Koganei

16. Tokyo 184-8588

17. Japan

Abstract

A new method of azide–alkyne cycloaddition (AAC) in the presence of Zn(OAc)₂ as an inexpensive and environmentally friendly catalyst in neat water has been developed.

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00787B

Reference54 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. Kinetics and Mechanism of 1,3-Dipolr Cycloadditions

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