83256-46-6Relevant articles and documents
Synthesis, anti-inflammatory, cytotoxic, and COX-1/2 inhibitory activities of cyclic imides bearing 3-benzenesulfonamide, oxime, and β-phenylalanine scaffolds: a molecular docking study
Abdel-Aziz, Alaa A.-M.,El-Azab, Adel S.,AlSaif, Nawaf A.,Alanazi, Mohammed M.,El-Gendy, Manal A.,Obaidullah, Ahmad J.,Alkahtani, Hamad M.,Almehizia, Abdulrahman A.,Al-Suwaidan, Ibrahim A.
, p. 610 - 621 (2020/02/15)
Cyclic imides containing 3-benzenesulfonamide, oxime, and β-phenylalanine derivatives were synthesised and evaluated to elucidate their in?vivo anti-inflammatory and ulcerogenic activity and in?vitro cytotoxic effects. Most active anti-inflammatory agents
Palladium-catalyzed intermolecular aminocarbonylation of alkenes: Efficient access of β-amino acid derivatives
Cheng, Jiashun,Qi, Xiaoxu,Li, Ming,Chen, Pinhong,Liu, Guosheng
supporting information, p. 2480 - 2483 (2015/03/04)
A novel palladium-catalyzed intermolecular aminocarbonylation of alkenes has been developed in which the employment of hypervalent iodine reagent can accelerate the intermolecular aminopalladation, which thus provides the successful catalytic transformation. The current transformation presents one of the most convenient methods to generate β-amino acid derivatives from simple alkenes.
Structural modifications of thalidomide produce analogs with enhanced tumor necrosis factor inhibitory activity
Muller,Corral,Shire,Wang,Moreira,Kaplan,Stirling
, p. 3238 - 3240 (2007/10/03)
-
