Divergent cyclization of 2-(5-iodo-1,2,3-triazolyl)benzamides toward triazole-fused lactams and cyclic imidates-Reference-Cited by-同舟云学术

Divergent cyclization of 2-(5-iodo-1,2,3-triazolyl)benzamides toward triazole-fused lactams and cyclic imidates

Published:2023 Issue:26 Volume:47 Page:12239-12247
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kotovshchikov Yury N.¹^ORCID,Tatevosyan Stepan S.¹,Latyshev Gennadij V.¹,Kugusheva Zoya R.¹,Lukashev Nikolay V.¹,Beletskaya Irina P.¹^ORCID

Affiliation:

1. Chemistry Department, M. V. Lomonosov Moscow State University, Leninskiye Gory 1/3, Moscow 119991, Russia

Abstract

Divergent approaches to 1,2,3-triazole-fused heterocyclesviachemoselective cyclization of 2-(5-iodotriazolyl)benzamides with controllable C–O or C–N bond formation have been developed.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ01264F

Reference96 articles.

1. An efficient one-pot synthesis of heterocycle-fused 1,2,3-triazole derivatives as anti-cancer agents

2. Intramolecular Azide−Alkyne Cycloaddition for the Fast Assembly of Structurally Diverse, Tricyclic 1,2,3-Triazoles

3. Synthesis and biological evaluation of triazolothienopyrimidine derivatives as novel HIV-1 replication inhibitors

4. Click chemistry and biocatalysis for the preparation of pancratistatin analogs

5. A Dipolar Cycloaddition Reaction To Access 6-Methyl-4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridines Enables the Discovery Synthesis and Preclinical Profiling of a P2X7 Antagonist Clinical Candidate

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