16715-03-0Relevant articles and documents
Addition of α-halocarboxylic acid esters to para-substituted benzaldehydes in the presence of pentacarbonyliron
Terent'ev,Vasil'eva,Kuz'mina,Mysova,Chakhovskaya
, p. 1273 - 1275 (2001)
Pentacarbonyliron promotes addition of α-halocarboxylic acid esters at the carbonyl group of benzaldehyde and its para-substituted analogs. The substituent in the benzene ring strongly affects the process.
(Z)-α-haloacrylates: An exceptionally stereoselective preparation via Cr(II)-mediated olefination of aldehydes with trihaloacetates
Barma,Kundu, Abhijit,Zhang, Hongming,Mioskowski, Charles,Falck
, p. 3218 - 3219 (2007/10/03)
(Z)-α-Fluoro-, (Z)-α-chloro-, and (Z)-α-bromoacrylates were obtained with unprecedented yield and stereocontrol (>99%) via addition of the corresponding commercial trihaloacetates to aldehydes at room temperature using stoichiometric Cr(II) salts or catal
Chain Reactions Induced by Cathodic Reduction
Shono, Tatsuya,Kise, Naoki,Masuda, Mitsuharu,Suzumoto, Takeshi
, p. 2527 - 2533 (2007/10/02)
Cathodic reduction of a system comprising carbon tetrachloride, chloroform, and an aldehyde led to an effective anionic chain reaction.The best current efficiency observed was about 1*104 percent .Such a chain reaction is an effective synthetic method for 1,1,1-trichloro-2-alkanols.The reaction system consisting of methyl trichloroacetate, methyl dichloroacetate, and an aldehyde and several other systems also exhibited a similar pattern of chain reaction.