期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 19, 期 44, 页码 9746-9751出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob01860d
关键词
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资金
- National Natural Science Foundation of China [22178315, 22078298, 21978271]
- Natural Science Foundation of Zhejiang Province of China [LY19B060011, Y21B020027]
The asymmetric hydrogenation catalyzed by iridium/f-diaphos L1, L5 or L12 was successfully demonstrated for the first time, affording chiral alcohols with high conversions and moderate to excellent enantioselectivities. The protocol could be easily scaled up to gram-scale with a Turnover Number (TON) of 9700.
The iridium/f-diaphos L1, L5 or L12 catalyzed asymmetric hydrogenation of 2-imidazolyl aryl/alkyl ketones to afford two enantiomers of the desired chiral alcohols with high conversions (up to 99% yield) and moderate to excellent enantioselectivities (61% - >99% ee) was realized for the first time. This protocol could be easily conducted on a gram-scale with a TON of 9700.
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