Addition of methoxy(phenylthio)methyllithium to ketones, followed by rearrangement of the adducts, provides a new method for the preparation of α-(phenylthio)aldehydes. The rearrangement is stereospecific.
Ketones are converted into α-sulfenylated aldehydes with addition of one carbon atom via reaction with methoxyphenylthiomethyllithium followed by rearrangement of the adducts.
通过与甲氧基苯基硫代甲基锂反应,加成一个碳原子,将酮转化为α-亚磺酰化醛,然后重排加合物。
Groot, Aede de; Jansen, Ben J. M., Synthesis, 1985, # 4, p. 434 - 436
作者:Groot, Aede de、Jansen, Ben J. M.
DOI:——
日期:——
GROOT A.; JANSEN B. J. M., TETRAHEDRON LETT., 1981, 22 NO 9, 887-888