The ring closing under solid–liquid phase-transfer catalysis conditions (SL-PTC) of hydroxysulfonamides 7, bearing a leaving group in the ortho position of the aryl moiety, generates 2-substituted-3,4-dihydro-2H-1,4-benzoxazines 4 in good to excellent yields. In the case of hydroxysulfonamides 7 bearing a bromine or iodine atom as a leaving group, a copper(I) salt is used to enable the reaction to occur.

Synthesis of 2-substituted 3, 4-dihydro-2H-1,4-benzoxazines through ligandless copper-catalyzed cyclization of hydroxysulfonamides under phase-transfer catalysis conditions

Penso M;
2008

Abstract

The ring closing under solid–liquid phase-transfer catalysis conditions (SL-PTC) of hydroxysulfonamides 7, bearing a leaving group in the ortho position of the aryl moiety, generates 2-substituted-3,4-dihydro-2H-1,4-benzoxazines 4 in good to excellent yields. In the case of hydroxysulfonamides 7 bearing a bromine or iodine atom as a leaving group, a copper(I) salt is used to enable the reaction to occur.
2008
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/71492
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