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• W2028771003 startingPage "8089" @default.
• W2028771003 abstract "A convenient and efficient synthesis of substituted dihydrofurans is developed via ring-enlargement of 1-dimethylaminopropenoyl-1-carbamoyl/benzoyl cyclopropanes catalyzed by ammonium acetate in acetic acid with high regio- and stereoselectivity. Some of the newly synthesized substituted dihydrofurans are subjected to further synthetic transformation in the presence of NaOH (aq) in ethanol to afford the corresponding 5-aryl-2,3-dihydrofuro[3,2-c]pyridin-4(5H)-ones in high yields." @default.
• W2028771003 created "2016-06-24" @default.
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• W2028771003 creator A5065037360 @default.
• W2028771003 date "2008-09-18" @default.
• W2028771003 modified "2023-10-09" @default.
• W2028771003 title "Ring-Enlargement of Dimethylaminopropenoyl Cyclopropanes: An Efficient Route to Substituted 2,3-Dihydrofurans" @default.
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• W2028771003 doi "https://doi.org/10.1021/jo801289p" @default.
• W2028771003 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18798678" @default.
• W2028771003 hasPublicationYear "2008" @default.
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