Cyclodehydration of gamma-hydroxy-beta-enaminoketones derived from 5-substituted-3-isoxazolmethanols leads to 3(2H)-furanones or3(2H) iminofuranes depending on the substitution pattern or the reaction conditions.

Cyclodehydration of γ-hydroxy-β-enaminoketones derived from 5-substituted-3-isoxazolemethanols leads to 3(2H)furanones or 3(2H)imino-furanes depending on the substitution pattern and on the reaction conditions. © 1984.

Ethyl 5-substituted-3-isoxazole carboxvyates as starting materials for a convenient route to 3(2H )-furanones and 3(2H )-iminofuranes

BARALDI, Pier Giovanni;BENETTI, Simonetta;MANFREDINI, Stefano;POLLINI, Gian Piero;SIMONI, Daniele
1984

Abstract

Cyclodehydration of γ-hydroxy-β-enaminoketones derived from 5-substituted-3-isoxazolemethanols leads to 3(2H)furanones or 3(2H)imino-furanes depending on the substitution pattern and on the reaction conditions. © 1984.
1984
Baraldi, Pier Giovanni; Barco, Achille; Benetti, Simonetta; Manfredini, Stefano; Pollini, Gian Piero; Simoni, Daniele
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/460275
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