Carbonyl and olefin reactivities for the Baylis–Hillman reaction of fluorocarbonyls
作者:P. Veeraraghavan Ramachandran、M. Venkat Ram Reddy、Michael T. Rudd
DOI:10.1039/b009177b
日期:——
The product formation and yields for the Baylis–Hillman reaction of fluorine-containing carbonyl compounds depend on a balance between the reactivities of the carbonyl and olefin partners.
作者:P. Veeraraghavan Ramachandran、M. Venkat Ram Reddy、Michael T. Rudd、Javier Read de Alaniz
DOI:10.1016/s0040-4039(98)01974-1
日期:1998.11
Ethyl acrylate and acrylonitrile fail to undergo efficient Baylis-Hillman reaction with fluoral, but provide good yields of products with pentafluorobenzaldehyde. Alternately, unsubstituted and beta-substituted [alpha- (ethoxycarbonyl)vinyl]aluminum react with perfluoroalkyl and -aryl aldehydes and ketones to provide the alpha-hydroxyalkenylated fluoroorganic compounds in good to excellent yields. (C) 1998 Elsevier Science Ltd. All rights reserved.
Study of Fluorocarbonyls for the Baylis−Hillman Reaction
作者:M. Venkat Ram Reddy、Michael T. Rudd、P. Veeraraghavan Ramachandran
DOI:10.1021/jo025591l
日期:2002.7.1
A study of the effect of fluorine substitution in Baylis-Hillman reactions of various fluorocarbonyl partners with acrolein, methyl vinyl ketone, ethyl acrylate, and acrylonitrile has been made.