摘要
The addition teaction of Grignard reagents to a-cinnamoyl ketene (1, 2-ethylene) dithioncetals 4 was examined.The results showed that the 1, 4-manner nucleoohilie attack at the cinnamoyl carbon double bond occurred. Possihle mechanism about the reaction selectivity is discussed.
The addition teaction of Grignard reagents to a-cinnamoyl ketene (1, 2-ethylene) dithioncetals 4 was examined.The results showed that the 1, 4-manner nucleoohilie attack at the cinnamoyl carbon double bond occurred. Possihle mechanism about the reaction selectivity is discussed.