Journal
ACS OMEGA
Volume 6, Issue 15, Pages 10415-10427Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c00868
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Funding
- National Natural Science Foundation of China [21962004, 21562004]
- Jiangxi provincial department of science and technology [20192BAB203004]
- emergency research project for Gannan Medical University [YJ202027]
- Fundamental Research Funds for Gannan Medical University [QD201810]
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The iridium-catalyzed transfer hydrogenation of N-heteroarenes enables the synthesis of substituted 1,2,3,4-tetrahydroquinoline derivatives in excellent yields, with broad functional group compatibility and the ability to achieve high enantioselectivity in chiral products.
An iridium-catalyzed transfer hydrogenation of N-heteroarenes to access a series of substituted 1,2,3,4-tetrahydroquinoline derivatives in excellent yields is disclosed. This transformation is distinguished with water-soluble and air-stable iridium complexes as the catalyst, formic acid as the hydrogen source, mild reaction conditions, and broad functional group compatibility. Most importantly, a tentative chiral N,N-chelated Cp*Ir(III) complex-catalyzed enantioselective transfer hydrogenation is also presented, affording chiral products in excellent yields and good enantioselectivities.
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