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Mendeleev Commun., 1998, том 8, выпуск 4, страницы 133–134 (Mi mendc4691)

Эта публикация цитируется в 13 статьях

One-step route to fluorinated furo[2,3-b]quinoxalines

V. N. Charushina, G. A. Mokrushinaa, G. M. Petrovaa, G. G. Alexandrova, O. N. Chupakhinb

a Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
b I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

Аннотация: The reaction of 6,7-difluoro-1-ethylquinoxalinium salts with 2,4-pentanedione, ethyl and bornyl acetoacetates and other β-keto esters results in the formation of 6,7-difluoro-3a,4,9,9a-tetrahydrofuro[2,3-b]quinoxalines. In addition, asymmetric 6-fluoro-7-morpholino and 6-fluoro-7-thiomorpholino substituted 1-ethylquinoxalinium salts react with alkyl acetoacetates in a regio- and stereoselective manner, thus giving exclusively the corresponding alkyl 2-methyl-6-fluoro-7-substituted 3a,4,9,9a-tetrahydrofuro[2,3-b]quinoxalin-3-carboxylates.

Язык публикации: английский

DOI: 10.1070/MC1998v008n04ABEH000973



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