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Direct (het)arylation of [1,2,4]triazolo[1,5-a]pyrimidines: Both eliminative and oxidative pathways
Research output
:
Contribution to journal
›
Article
›
peer-review
Institute of Chemical Engineering
Institute of Physics and Technology
Innovation and Implementation Center for Irradiation Sterilization
Department of Organic and Biomolecular Chemistry
Department of Technology of Organic Synthesis
Overview
Cite this
DOI
https://doi.org/10.1016/j.tet.2017.07.042
Final published version
Nikolay A. Rasputin
Nadezhda S. Demina
Roman A. Irgashev
Gennady L. Rusinov
Oleg N. Chupakhin
Valery N. Charushin
Original language
English
Pages (from-to)
5500-5508
Number of pages
9
Journal
Tetrahedron
Volume
73
Issue number
37
DOIs
https://doi.org/10.1016/j.tet.2017.07.042
Publication status
Published -
14 Sept 2017
ASJC Scopus subject areas
Biochemistry
Drug Discovery
Organic Chemistry
Research areas
(Het)aryl magnesium bromide, Direct (het)arylation, Nucleophilic aromatic substitution of hydrogen (S), [1,2,4]Triazolo[1,5-a]pyrimidine
WoS ResearchAreas Categories
Chemistry, Organic
ID: 2042696
