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Mingxin Chang, Ph.D.

Affiliations: 
2013 Graduate School - New Brunswick Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Synthetic organic, inorganic and organometallic chemistry
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"Mingxin Chang"
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Xumu Zhang grad student 2013 Rutgers, New Brunswick
 (Transition metal-catalyzed asymmetric hydrogenation for synthesis of chiral amines.)
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Publications

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Zhao W, Wang W, Zhou H, et al. (2023) An Asymmetric Hydrogenation/N-Alkylation Sequence for a Step-Economical Route to Indolizidines and Quinolizidines. Angewandte Chemie (International Ed. in English). e202308836
Xie R, Zhou H, Lu H, et al. (2022) Transition-Metal-Catalyzed Asymmetric Reductive Amination and Amidation Cascade Reaction for the Synthesis of Piperazinones. Organic Letters
Xie R, Liu C, Lin R, et al. (2022) 1,2-Diamines as the Amine Sources in Amidation and Rhodium-Catalyzed Asymmetric Reductive Amination Cascade Reactions. Organic Letters. 24: 5646-5650
Wu Z, Wang W, Guo H, et al. (2022) Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources. Nature Communications. 13: 3344
Gao Z, Liu J, Huang H, et al. (2021) An Iridium Catalytic System Compatible with Inorganic and Organic Nitrogen Sources for Dual Asymmetric Reductive Amination Reactions. Angewandte Chemie (International Ed. in English)
Yuan S, Gao G, Wang L, et al. (2020) The combination of asymmetric hydrogenation of olefins and direct reductive amination. Nature Communications. 11: 621
Wu Z, Du S, Gao G, et al. (2019) Secondary amines as coupling partners in direct catalytic asymmetric reductive amination. Chemical Science. 10: 4509-4514
Zhou H, Zhao W, Zhang T, et al. (2019) Enantioselective Synthesis of 2-Substituted Pyrrolidines via Intramolecular­ Reductive Amination Synthesis. 51: 2713-2719
Gao G, Du S, Yang Y, et al. (2018) Direct Asymmetric Reductive Amination for the Synthesis of ()-Rivastigmine. Molecules (Basel, Switzerland). 23
Huang H, Zhao Y, Yang Y, et al. (2017) Direct Catalytic Asymmetric Reductive Amination of Aliphatic Ketones Utilizing Diphenylmethanamine as Coupling Partner. Organic Letters
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