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Iridium-Catalyzed Asymmetric Transfer Hydrogenation of 1-Aryl-1-alkylethenes with Ethanol
被引:4
|作者:
Tang, Xixia
[1
]
Qian, Lu
[2
]
Liu, Guixia
[3
]
Huang, Zheng
[2
,3
]
机构:
[1] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, Hangzhou 310024, Peoples R China
[3] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金:
中国国家自然科学基金;
关键词:
ENANTIOSELECTIVE HYDROGENATION;
LIGANDS;
COMPLEXES;
OLEFINS;
SESQUITERPENES;
DERIVATIVES;
D O I:
10.1021/acs.orglett.3c01880
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Asymmetrictransfer hydrogenation of 1-aryl-1-alkylethenes withethanol was developed with a chiral (PCN)Ir complex as the precatalyst,featuring high enantioselectivities, good functional group tolerance,and operational simplicity. The method is further applied to formalintramolecular asymmetric transfer hydrogenation of alkenols withoutan external H-donor, producing a tertiary stereocenter and remoteketone group simultaneously. The utility of the catalytic system washighlighted by gram scale synthesis and the synthesis of the key precursorof (R)-xanthorrhizol.
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页码:4950 / 4954
页数:5
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