-Benzyl aldehydes are prepared from easily available -silylalkenals and fluoride reagents, under mild experimental conditions; the reaction occurs instantaneously with almost quantitative yields. A plausible mechanism is suggested, which involves a 1,2-phenyl migration from the silicon to the adjacent carbon atom.
New synthesis of α-benzylaldehydes from 2-(dimethylphenylsilylmethylene)alkanals by fluoride promoted phenyl migration
ARONICA, LAURA ANTONELLA;
2002-01-01
Abstract
-Benzyl aldehydes are prepared from easily available -silylalkenals and fluoride reagents, under mild experimental conditions; the reaction occurs instantaneously with almost quantitative yields. A plausible mechanism is suggested, which involves a 1,2-phenyl migration from the silicon to the adjacent carbon atom.File in questo prodotto:
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