Substituent effects on stereoselectivity of dihalocarbene reactions with cyclohexadiene and on the reactivity of bis-dihalocyclopropanes in electrophilic nitrations en route to pyrimidine N-oxides
Author:
Affiliation:
1. Lomonosov Moscow State University
2. Department of Chemistry
3. Moscow 119991
4. Russia
5. IPhAc RAS
6. Department of Chemistry & Biochemistry
7. Florida State University
8. Tallahassee
9. USA
Abstract
Bis-adducts of cyclohexa-1,4-diene with dihalocarbenes were synthesized and investigated in heterocyclization.
Funder
Division of Chemistry
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/2017/OB/C7OB02463K
Reference54 articles.
1. G. W. Rewcastle , Pyrimidines and their Benzo Derivatives , in Comprehensive Heterocyclic Chemistry III , ed. A. R. Katritzky , C. A. Ramsden , E. F. V. Scriven , R. J. K. Taylor , Elsevier Ltd. , Oxford , 2008 , vol. 8 , pp. 120–27
2. Significance and Biological Importance of Pyrimidine in the Microbial World
3. Pyrimidine-based antimalarials: design strategies and antiplasmodial effects
4. Design, synthesis, and biological evaluation of novel quinazolinyl-diaryl urea derivatives as potential anticancer agents
5. 2,4-Diaminopyrimidines as dual ligands at the histamine H 1 and H 4 receptor—H 1 /H 4 -receptor selectivity
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