451492-17-4Relevant academic research and scientific papers
Base-promoted regiodivergent allylation of: N -acylhydrazones with Morita-Baylis-Hillman carbonates by tuning the catalyst
Sun, Fang,Yin, Tingrui,Feng, Anni,Hu, Yong,Yu, Chenxia,Li, Tuanjie,Yao, Changsheng
, p. 5283 - 5293 (2019/06/07)
A regiodivergent allylation of N-acylhydrazones with Morita-Baylis-Hillman (MBH) carbonates has been developed, providing α- or γ-allylated products in excellent yields by using different catalysts. The nature of the base catalyst plays a pivotal role in
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.
Synthesis of unsaturated β-amino acid derivatives from carbamates of the Baylis-Hillman products
Ciclosi, Marco,Fava, Cristiana,Galeazzi, Roberta,Orena, Mario,Sepulveda-Arques, José
, p. 2199 - 2202 (2007/10/03)
By treatment with a catalytic amount of DBU in DCM, N-p-toluenesulphonyl carbamates 6a-c, prepared starting from the corresponding Baylis-Hillman adducts, gave (E)-2-(p-toluenesulphonylaminomethyl)propenoates 3a-c, exclusively. On the contrary, changing D
