Chiral 1,5-disubstituted 1,2,3-triazoles – versatile tools for foldamers and peptidomimetic applications-Reference-Cited by-同舟云学术

Chiral 1,5-disubstituted 1,2,3-triazoles – versatile tools for foldamers and peptidomimetic applications

Published:2020 Issue:10 Volume:18 Page:1957-1967
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Said Stålsmeden Anna¹²³⁴^ORCID,Paterson Andrew J.¹²³⁴^ORCID,Szigyártó Imola Cs.⁵⁶⁷⁸^ORCID,Thunberg Linda⁹¹⁰¹¹¹²¹³^ORCID,Johansson Johan R.¹⁴¹⁵¹⁶¹¹¹²^ORCID,Beke-Somfai Tamás⁵⁶⁷⁸^ORCID,Kann Nina¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry and Chemical Engineering

2. Chalmers University of Technology

3. SE-41296 Göteborg

4. Sweden

5. Research Centre for Natural Sciences

6. Hungarian Academy of Sciences

7. H-1117 Budapest

8. Hungary

9. Early Chemical Development

10. Pharmaceutical Sciences

11. BioPharmaceuticals R&D

12. AstraZeneca

13. Gothenburg

14. Medicinal Chemistry

15. Research and Early Development Cardiovascular

16. Renal and Metabolism

Abstract

Eight chiral triazoles, for use as peptidomimetic building blocks, were prepared using the ruthenium-catalyzed click (RuAAC) reaction and their conformational properties evaluated by quantum chemistry.

Funder

Vetenskapsrådet

Svenska Forskningsrådet Formas

Carl Tryggers Stiftelse för Vetenskaplig Forskning

Magyar Tudományos Akadémia

H2020 Marie Skłodowska-Curie Actions

Országos Tudományos Kutatási Alapprogramok

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

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