Studies on the synthesis of 1′-CN-triazolyl-<i>C</i>-ribosides-Reference-Cited by-同舟云学术

Studies on the synthesis of 1′-CN-triazolyl-C-ribosides

Published:2022 Issue:36 Volume:20 Page:7261-7269
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Bozinovic Nina¹,Aguiar Viviane Marques de²,Ferry Angélique¹,Gallier Florian¹^ORCID,Lubin-Germain Nadège¹,Uziel Jacques¹,Miranda Leandro Soter de Mariz e¹²^ORCID

Affiliation:

1. CY Cergy Paris Université, CNRS, BioCIS, 95000, Cergy-Pontoise, France

2. Biocatalysis and Organic Synthesis Group, Universidade Federal do Rio de Janeiro, Av Athos da Silveira Ramos 149, Centro de Tecnologia, Bl A, 21941909 Ilha do Fundão, Rio de Janeiro, Brazil

Abstract

Synthesis of the C1′–CN -1,2,3-triazolyl-C-ribonucleosides was achieved through the cyanation of the corresponding alkynyl-C-riboside. A new spirocyclic guanosine analogue is reported through the amination of the 1′-CN-triazolyl-C-riboside.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01403C

Reference25 articles.

1. Synthesis of C-Ribosyl-1,2,3-triazolyl Carboxamides

2. Functionalization of 2H-1,2,3-Triazole C-Nucleoside Template via N2 Selective Arylation

3. Synthesis of ribavirin 2’-Me-C-nucleoside analogues

4. Huisgen Cycloaddition Reaction of C-Alkynyl Ribosides under Micellar Catalysis: Synthesis of Ribavirin Analogues

5. Synthesis and antitumor activities investigation of a C-nucleoside analogue of ribavirin

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Developments in the chemistry and biology of 1,2,3‐triazolyl‐C‐nucleosides;Archiv der Pharmazie;2023-12-27

2. Five-membered ring systems: with more than one N atom;Progress in Heterocyclic Chemistry;2023