The Reaction of Ketenes with Grignard Reagents
CD Hurd, RN Jones, FH Blunck
Index: Hurd; Jones; Blunck Journal of the American Chemical Society, 1935 , vol. 57, p. 2033,2035
Full Text: HTML
Citation Number: 6
Abstract
Diphenylketen e and phenylmagnesium bromide react'to produce a derivative of triphenylvinyl alcohol. With ketene2 itself, the course of the Grignard reaction has not been established because of the vigor and complexity of the process. Toward the dimer of dimethylketene, ethylmagnesium bromide3 adds to give the cyclic glycol in high yields
Related Articles:
Synthetic scope of the triethyloxonium ion catalyzed homologation of ketones with diazoacetic esters
[Mock,W.L.; Hartman,M.E. Journal of Organic Chemistry, 1977 , vol. 42, p. 459 - 465]