2001Synthetic CommunicationsRequires access

NEW DIHYDROFURAN AND DIHYDROPYRAN DERIVATIVES BY IODOENOLCYCLIZATION OF 2-PRENYL-1,3-DICARBONYL COMPOUNDS: STUDIES ON THE REGIOCHEMISTRY

Roberto Antonioletti, F. D'ONOFRIO, Barbara Rossi

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Abstract

Both dihydrofuran and dihydropyran derivatives are obtained performing iodoenolcyclization of 2-alkenyl-1,3-dicarbonyl compounds having a highly substituted double bond. The regiochemistry is greatly dependent on the nature of carbonyl groups.

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What this paper is about

Both dihydrofuran and dihydropyran derivatives are obtained performing iodoenolcyclization of 2-alkenyl-1,3-dicarbonyl compounds having a highly substituted double bond. The regiochemistry is greatly dependent on the nature of carbonyl groups.

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OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Both dihydrofuran and dihydropyran derivatives are obtained performing iodoenolcyclization of 2-alkenyl-1,3-dicarbonyl compounds having a highly substituted double bond. The regiochemistry is greatly dependent on the nature of carbonyl groups.

Key concepts: Dihydropyran, Regioselectivity, Chemistry, Prenylation, Double bond, Stereochemistry, Organic chemistry, Catalysis

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NEW DIHYDROFURAN AND DIHYDROPYRAN DERIVATIVES BY IODOENOLCYCLIZATION OF 2-PRENYL-1,3-DICARBONYL COMPOUNDS: STUDIES ON THE REGIOCHEMISTRY — Research Paper | ScholarLens