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.File in questo prodotto:
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