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• W2023865097 abstract "Deprotonation of 2-(phenylsulfonyl)-1,3-oxazole (1) readily provides a useful C-5 carbanion that is reactive with a variety of electrophiles. Aldehydes and ketones are useful substrates, and the formation of 5-iodo- and 5-tri-n-butylstannyl oxazoles affords access to cross-coupling reactions. Subsequent nucleophilic displacement of the 2-phenylsulfonyl group provides a general route for the synthesis of 2,5-disubstituted-1,3-oxazoles." @default.
• W2023865097 created "2016-06-24" @default.
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• W2023865097 date "2010-01-19" @default.
• W2023865097 modified "2023-10-16" @default.
• W2023865097 title "General Methodology for the Preparation of 2,5-Disubstituted-1,3-oxazoles" @default.
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• W2023865097 doi "https://doi.org/10.1021/ol902833p" @default.
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