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• W1969689368 abstract "A new family of optically active 2,3-dihydrobenzofurans has been prepared by a simple chemoenzymatic asymmetric strategy. This synthetic approach is based on the combination of a lipase-mediated kinetic resolution of 1-aryl-2-propanols or bioreduction of the corresponding ketones followed by an intramolecular cyclization reaction. These novel compounds have been prepared in enantiopure form and in good overall yield through a straightforward route." @default.
• W1969689368 created "2016-06-24" @default.
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• W1969689368 date "2010-07-15" @default.
• W1969689368 modified "2023-10-17" @default.
• W1969689368 title "Straightforward Synthesis of Enantiopure 2,3-Dihydrobenzofurans by a Sequential Stereoselective Biotransformation and Chemical Intramolecular Cyclization" @default.
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• W1969689368 doi "https://doi.org/10.1021/ol101336y" @default.
• W1969689368 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20670014" @default.
• W1969689368 hasPublicationYear "2010" @default.
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