Reactivity of the ester group attached isoxazoline, benzisoxazole, and isoxazole: A facial preparation of 3-acyl-substituted these heterocycles
A facile preparation of 3-acyl-substituted isoxazolines, benzisoxazoles, and isoxazoles from the corresponding 3-carboxylate esters is described. The process, involving reaction of the ester derivative of 3-carboxylic acid substituted heterocycles with Gr
Murai, Kenichi,Miyazaki, Shuji,Fujioka, Hiromichi
p. 3746 - 3749
(2012/10/07)
Ethyl 2,4-dioxoalkanoates as starting materials for a convenient route to 3(2H)furanones and 3(2H)furanimines
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Baraldi,Barco,Benetti,et al.
p. 235 - 242
(2007/10/02)
ETHYL 5-SUBSTITUTED-3-ISOXAZOLECARBOXYLATES AS STARTING MATERIALS FOR A CONVENIENT ROUTE TO 3(2H)FURANONES AND 3(2H)IMINOFURANES.
Cyclodehydration of γ-hydroxy-β-enaminoketones derived from 5-substituted-3-isoxazolemethanols leads to 3(2H)furanones or 3(2H)iminofuranes depending on the substitution pattern and on the reaction conditions.
Baraldi, Pier Giovanni,Barco, Achille,Benetti, Simonetta,Manfredini, Stefano,Pollini, Gian Piero,Simoni, Daniele
p. 4313 - 4316
(2007/10/02)
Convenient Synthesis of Alkyl Ketones from Carboxylic Esters
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Kikkawa, Ikuo,Yorifuji, Tadahiko
p. 877 - 880
(2007/10/02)
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