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New routes to 5-substituted oxazoles

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Publication details

JournalJournal of the Chemical Society-Perkin Transactions 1
DatePublished - 2000
Issue number4
Number of pages5
Pages (from-to)527-531
Original languageEnglish

Abstract

Ultrasound-promoted desulfonylation of 5-substituted 4-tosyloxazoles, prepared from tosylmethyl isocyanide and carboxylic acid chlorides or by dianion chemistry, leads to 5-monosubstituted oxazoles.

    Research areas

  • SYNTHETIC ORGANIC-CHEMISTRY, DESULFONYLATION, NEOOXAZOLOMYCIN, OXAZOLOMYCIN, MAGNESIUM, EFFICIENT

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