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Zhaobin Han

Showing results (1-10 of 26) with videos related to

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Chemistry, an Asian Journal|September 5, 2008
Spiro skeletons: a class of privileged structure for chiral ligand designKuiling Ding, Zhaobin Han, Zheng Wang
Angewandte Chemie (International Ed. in English)|March 9, 2013
The N-H functional group in organometallic catalysisBaoguo Zhao, Zhaobin Han, Kuiling Ding
Journal of the American Chemical Society|May 14, 2019
Ir-Catalyzed Double Asymmetric Hydrogenation of 3,6-Dialkylidene-2,5-diketopiperazines for Enantioselective Synthesis of Cyclic DipeptidesYao Ge, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|January 22, 2014
SpinPhox/iridium(I)-catalyzed asymmetric hydrogenation of cyclic α-alkylidene carbonyl compoundsXu Liu, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|June 18, 2009
Spiro[4,4]-1,6-nonadiene-based phosphine-oxazoline ligands for iridium-catalyzed enantioselective hydrogenation of ketiminesZhaobin Han, Zheng Wang, Xumu Zhang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 3, 2020
Iridium-Catalyzed Enantioselective Hydrogenation of Indole and Benzofuran DerivativesYao Ge, Zheng Wang, Zhaobin Han, et al.
Angewandte Chemie (International Ed. in English)|February 19, 2019
Lutidine-Based Chiral Pincer Manganese Catalysts for Enantioselective Hydrogenation of KetonesLinli Zhang, Yitian Tang, Zhaobin Han, et al.
Angewandte Chemie (International Ed. in English)|September 17, 2013
Spiro[4,4]-1,6-nonadiene-based diphosphine oxides in lewis base catalyzed asymmetric double-aldol reactionsPanke Zhang, Zhaobin Han, Zheng Wang, et al.
Accounts of Chemical Research|January 14, 2021
A Type of Structurally Adaptable Aromatic Spiroketal Based Chiral Diphosphine Ligands in Asymmetric CatalysisXiaoming Wang, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|May 26, 2020
Manganese-Catalyzed anti-Selective Asymmetric Hydrogenation of α-Substituted β-KetoamidesLinli Zhang, Zheng Wang, Zhaobin Han, et al.
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Showing results (1-10 of 26) with videos related to

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Pageof 3
Chemistry, an Asian Journal|September 5, 2008
Spiro skeletons: a class of privileged structure for chiral ligand designKuiling Ding, Zhaobin Han, Zheng Wang
Angewandte Chemie (International Ed. in English)|March 9, 2013
The N-H functional group in organometallic catalysisBaoguo Zhao, Zhaobin Han, Kuiling Ding
Journal of the American Chemical Society|May 14, 2019
Ir-Catalyzed Double Asymmetric Hydrogenation of 3,6-Dialkylidene-2,5-diketopiperazines for Enantioselective Synthesis of Cyclic DipeptidesYao Ge, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|January 22, 2014
SpinPhox/iridium(I)-catalyzed asymmetric hydrogenation of cyclic α-alkylidene carbonyl compoundsXu Liu, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|June 18, 2009
Spiro[4,4]-1,6-nonadiene-based phosphine-oxazoline ligands for iridium-catalyzed enantioselective hydrogenation of ketiminesZhaobin Han, Zheng Wang, Xumu Zhang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 3, 2020
Iridium-Catalyzed Enantioselective Hydrogenation of Indole and Benzofuran DerivativesYao Ge, Zheng Wang, Zhaobin Han, et al.
Angewandte Chemie (International Ed. in English)|February 19, 2019
Lutidine-Based Chiral Pincer Manganese Catalysts for Enantioselective Hydrogenation of KetonesLinli Zhang, Yitian Tang, Zhaobin Han, et al.
Angewandte Chemie (International Ed. in English)|September 17, 2013
Spiro[4,4]-1,6-nonadiene-based diphosphine oxides in lewis base catalyzed asymmetric double-aldol reactionsPanke Zhang, Zhaobin Han, Zheng Wang, et al.
Accounts of Chemical Research|January 14, 2021
A Type of Structurally Adaptable Aromatic Spiroketal Based Chiral Diphosphine Ligands in Asymmetric CatalysisXiaoming Wang, Zhaobin Han, Zheng Wang, et al.
Angewandte Chemie (International Ed. in English)|May 26, 2020
Manganese-Catalyzed anti-Selective Asymmetric Hydrogenation of α-Substituted β-KetoamidesLinli Zhang, Zheng Wang, Zhaobin Han, et al.
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