Rhodium-Catalyzed Asymmetric Hydrogenation of 3-Benzoylaminocoumarins for the Synthesis of Chiral 3-Amino Dihydrocoumarins

被引:25
作者
Xu, Yunnan [1 ]
Liu, Delong [1 ]
Deng, Yu [1 ]
Zhou, Yi [1 ]
Zhang, Wanbin [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, Sch Pharm, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
3-amino dihydrocoumarins; asymmetric hydrogenation; chirality; cyclic amino acid derivatives; rhodium; ENANTIOSELECTIVE SYNTHESES; BIOLOGICAL EVALUATION; DIPHOSPHINE LIGANDS; PHOSPHORUS LIGANDS; AMINO-ACIDS; INHIBITORS; DERIVATIVES; DISCOVERY; MECHANISM; INDOLINE;
D O I
10.1002/anie.202110286
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An asymmetric hydrogenation of 3-benzoylaminocoumarins was achieved for the first time using our BridgePhos-Rh catalytic system, providing chiral 3-amino dihydrocoumarins in high yields (up to 98 %) and with excellent enantioselectivities (up to 99.7 % ee). The relationship between the enantioselectivities of the hydrogenations and the dihedral angles and the resulting pi-pi stacking effects of the BridgePhos-Rh complexes, which were determined by X-ray diffraction analysis, are discussed. The corresponding hydrogenated products allow for many transformations, providing several chiral skeletons with important physiological and pharmacological activities.
引用
收藏
页码:23602 / 23607
页数:6
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