741716-65-4Relevant academic research and scientific papers
α-methylene-β-trichloroacetylamino alkanoates from trichloroacetimidates of the Baylis-Hillman adducts
Galeazzi, Roberta,Martelli, Gianluca,Orena, Mario,Rinaldi, Samuele
, p. 2560 - 2566 (2007/10/03)
The Baylis-Hillman adducts 1 were treated with a large amount of CCl 3CN in the presence of DBU without solvent to give in good yield the corresponding trichloroacetimidates 5 which by thermal [3.3]sigmatropic rearrangement were converted into
Stereoselective iodocyclization of 3-acylamino-2-methylene alkanoates: Synthesis of analogues of N-benzoyl-syn-phenylisoserine
Galeazzi, Roberta,Martelli, Gianluca,Mobbili, Giovanna,Orena, Mario,Rinaldi, Samuele
, p. 2571 - 2574 (2007/10/03)
(Matrix Presented) A convenient approach to racemic analogues of N-benzoyl-syn-phenylisoserine was realized via the stereoselective iodocyclization of amides obtained from Baylis-Hillman adducts.
