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
The role of the hydrogen bonding in cycloadditions of benzonitrile oxide with cyanophenols
ROMEO, Roberto
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 effectFile in questo prodotto:
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