A selective oxidation opening of the eterocyclic nucleus of 2-(acylmethyl)-5-methylfurans or 2-(5-methyl-2-furyl)-1,3-dicarbonyl compounds by m-chloroperbenzoic acid allows the one-pot synthesis of 3-(2H)-furanone derivatives. Synthesis of Fungal metabolite viridicatic acid.

A NEW APPROACH TO POLYFUNCTIONAL 3(2H)-FURANONES

ANTONIOLETTI R;
1988

Abstract

A selective oxidation opening of the eterocyclic nucleus of 2-(acylmethyl)-5-methylfurans or 2-(5-methyl-2-furyl)-1,3-dicarbonyl compounds by m-chloroperbenzoic acid allows the one-pot synthesis of 3-(2H)-furanone derivatives. Synthesis of Fungal metabolite viridicatic acid.
1988
Furans
m-chloroperbenzoic acid
3-(2H)-furanones
viridicatic acid
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/268811
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact