New routes to 5-substituted oxazoles

Autor: Richard J. K. Taylor, Matthew S. Addie
Rok vydání: 2000
Předmět:
Zdroj: Journal of the Chemical Society, Perkin Transactions 1. :527-531
ISSN: 1364-5463
1470-4358
DOI: 10.1039/a908987j
Popis: 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.
Databáze: OpenAIRE