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Coupling of Styrylmalonates with Furan and Benzofuran Carbaldehydes: Synthesis and Chemistry of Substituted (4-Oxocyclopent-2-enyl)malonates Full article

Journal Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263
Output data Year: 2021, Volume: 86, Number: 12, Pages: 8489-8499 Pages count : 11 DOI: 10.1021/acs.joc.1c00536
Authors Borisov Denis D. 1 , Chermashentsev Grigorii R. 1 , Novikov Roman A. 1 , Tomilov Yury V. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation

Abstract: On the basis of the reaction of β-styrylmalonates with furfural derivatives in the presence of GaCl3 that occurs with opening of the furan ring, an efficient diastereoselective method for the synthesis of trisubstituted cyclopentenones containing a 1,4-diketone moiety was developed. The regularities of the reaction were studied, and a number of chemical reactions of the resulting substrates were carried out. A mechanism for the formation of substituted (4-oxo-2-arylcyclopent-2-enyl)malonates was suggested.
Cite: Borisov D.D. , Chermashentsev G.R. , Novikov R.A. , Tomilov Y.V.
Coupling of Styrylmalonates with Furan and Benzofuran Carbaldehydes: Synthesis and Chemistry of Substituted (4-Oxocyclopent-2-enyl)malonates
Journal of Organic Chemistry. 2021. V.86. N12. P.8489-8499. DOI: 10.1021/acs.joc.1c00536 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000664332300052
≡ Scopus: 2-s2.0-85108448527
≡ OpenAlex: W3165259061
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