An Improved Synthesis of 2-Substituted-3-furoic Acids Leading to an Intramolecular Diels-Alder Reaction Between a Dienophile and Furan Diene Both Containing an Electron Withdrawing Group

DOI: 10.1039/P19920002729

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 2729 - 2734 (1992)

Update date:2022-08-04

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Authors:

Yu, Shuyuan

Beese, Giovanna

Keay, Brian A.

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Article abstract of DOI:10.1039/P19920002729

An improved preparation of various 2-substituted-3-furoic acids by lithiation of 2-methyl-3-furoic acid with 2.0 equiv. of butyllithium, and a successful intramolecular Diels-Alder reaction using 0.1 equiv. of methylaluminium dichloride between a dienophi

Full text of DOI:10.1039/P19920002729

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