Chemistry of 5-oxodihydroisoxazoles .18. Synthesis of oxazoles by the photolysis and pyrolysis of 2-acyl-5-oxo-2,5-dihydroisoxazoles


Autoria(s): Prager, RH; Smith, JA; Weber, B; Williams, CM
Data(s)

01/01/1997

Resumo

N-Acylisoxazol-5-ones lose carbon dioxide under photochemical and thermal conditions affording iminocarbenes which undergo intramolecular cyclisation through the oxygen of the acyl group to give oxazoles. Under photochemical conditions those acylisoxazolones with electron withdrawing groups at C-4 usually give high yields of oxazoles, while those with electron donating groups at C-4 give only poor yields: the reverse is observed under thermal conditions.

Identificador

http://espace.library.uq.edu.au/view/UQ:57875

Idioma(s)

eng

Palavras-Chave #Chemistry, Organic #Nudibranch Eggmasses #Marine Sponge #Thiazoles
Tipo

Journal Article