Metal carbonyl mediated rearrangement of 5-(2-oxoalkyl)-1,2,4-oxadiazoles: synthesis of fully substituted pyrimidines
Author:
Affiliation:
1. St Petersburg State University, Institute of Chemistry, 7/9 Universitetskaya nab., St Petersburg, 199034, Russia
Abstract
Funder
Russian Science Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00148B
Reference40 articles.
1. Pyridine and Pyrimidine Derivatives as Privileged Scaffolds in Biologically Active Agents
2. An overview of the synthetic route to the marketed formulations of pyrimidine: A Review
3. Synthesis, anti-microbial activity, cytotoxicity of some novel substituted (5-(3-(1H-benzo[d]imidazol-2-yl)-4-hydroxybenzyl)benzofuran-2-yl)(phenyl)methanone analogs
4. An overview on synthesis and biological activity of pyrimidines
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