959799-63-4Relevant academic research and scientific papers
Rhodium-catalyzed asymmetric addition of arylboronic acids to γ-phthalimido-substituted-α,β-unsaturated carboxylic acid esters: An approach to γ-amino acids
Han, Fuzhong,Chen, Jun,Zhang, Xiangyang,Liu, Jibing,Cun, Linfeng,Zhu, Jin,Deng, Jingen,Liao, Jian
, p. 830 - 833 (2011)
Efficient Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to ethyl-γ-phthalimidocrotonate by using bis-sulfoxide ligand affords γ-aminobutyric acid (GABA) derivatives with high enantioselectivities (90-96% ee) under mild conditions. Optically pu
Enantioselective synthesis of β-aryl-γ-amino acid derivatives via Cu-catalyzed asymmetric 1,4-reductions of γ-phthalimido-substituted α,β-unsaturated carboxylic acid esters
Deng, Jun,Hu, Xiang-Ping,Huang, Jia-Di,Yu, Sai-Bo,Wang, Dao-Yong,Duan, Zheng-Chao,Zheng, Zhuo
, p. 6022 - 6024 (2008/12/22)
(Chemical Equation Presented) A series of chiral β-aryl-substituted γ-amino butyric acid derivatives were synthesized in good enantioselectivities via the Cu-catalyzed asymmetric conjugate reduction of γ-ph-thalimido-α,β-unsaturated carboxylic acid esters
