The reactivity of aromatic nitriles in cycloadditions with benzonitrile oxide is remarkably enhanced by the ortho-hydroxy substituent. Semiempirical PM3 calculations are in agreement with a hydrogen bonding effect. Copyright (C) 1996 Elsevier Science Ltd
The role of the hydrogen bonding in cycloadditions of benzonitrile oxide with cyanophenols.
CHIACCHIO, Ugo;PERRINI, Giancarlo;PISTARA', Venerando;
1996-01-01
Abstract
The reactivity of aromatic nitriles in cycloadditions with benzonitrile oxide is remarkably enhanced by the ortho-hydroxy substituent. Semiempirical PM3 calculations are in agreement with a hydrogen bonding effect. Copyright (C) 1996 Elsevier Science LtdFile in questo prodotto:
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