Zhang M, Wang H, Shan H, Xi L, Lu C, Du X
Nat Commun. 2025; 16(1):2505.
PMID: 40082430
PMC: 11906793.
DOI: 10.1038/s41467-025-57804-8.
Teng Y, Yang H, Tian Y
Molecules. 2024; 29(17).
PMID: 39274956
PMC: 11397416.
DOI: 10.3390/molecules29174109.
Li B, Wang Z, Luo Y, Wei H, Chen J, Liu D
Nat Commun. 2024; 15(1):5482.
PMID: 38942809
PMC: 11213955.
DOI: 10.1038/s41467-024-49801-0.
Lu Y, Che C, Zhen G, Chang X, Dong X, Wang C
Chem Sci. 2024; 15(17):6507-6514.
PMID: 38699278
PMC: 11062095.
DOI: 10.1039/d4sc00667d.
He J, Li Z, Li R, Kou X, Liu D, Zhang W
Adv Sci (Weinh). 2024; 11(23):e2400621.
PMID: 38509867
PMC: 11187880.
DOI: 10.1002/advs.202400621.
Diastereoselective Hydrogenation of Tetrasubstituted Olefins using a Heterogeneous Pt-Ni Alloy Catalyst.
Swann W, Yadav A, Colvin N, Freundl N, Li C
Angew Chem Int Ed Engl. 2024; 63(19):e202317710.
PMID: 38407502
PMC: 11098551.
DOI: 10.1002/anie.202317710.
Thermodynamic evaluations of the acceptorless dehydrogenation and hydrogenation of pre-aromatic and aromatic N-heterocycles in acetonitrile.
Qian B, Wang X, Wang Q, Zhu X, Shen G
RSC Adv. 2024; 14(1):222-232.
PMID: 38173608
PMC: 10758765.
DOI: 10.1039/d3ra08022f.
Expedient and divergent synthesis of unnatural peptides through cobalt-catalyzed diastereoselective umpolung hydrogenation.
Song X, Bai S, Li Y, Yi T, Long X, Pu Q
Sci Adv. 2023; 9(51):eadk4950.
PMID: 38117889
PMC: 10732522.
DOI: 10.1126/sciadv.adk4950.
Bulky, electron-rich, renewable: analogues of Beller's phosphine for cross-couplings.
van der Westhuizen D, Castro A, Hazari N, Gevorgyan A
Catal Sci Technol. 2023; 13(23):6733-6742.
PMID: 38026730
PMC: 10680433.
DOI: 10.1039/d3cy01375h.
Thermodynamic Evaluations of Amines as Hydrides or Two Hydrogen Ions Reductants and Imines as Protons or Two Hydrogen Ions Acceptors, as Well as Their Application in Hydrogenation Reactions.
Shen G, Qian B, Luo G, Fu Y, Zhu X
ACS Omega. 2023; 8(35):31984-31997.
PMID: 37692224
PMC: 10483529.
DOI: 10.1021/acsomega.3c03804.
Asymmetric arene hydrogenation: towards sustainability and application.
Luckemeier L, Pierau M, Glorius F
Chem Soc Rev. 2023; 52(15):4996-5012.
PMID: 37427715
PMC: 10389296.
DOI: 10.1039/d3cs00329a.
Asymmetric hydrogenation of 1,1-diarylethylenes and benzophenones through a relay strategy.
Li K, Wu W, Lin Y, Shi H
Nat Commun. 2023; 14(1):2170.
PMID: 37061515
PMC: 10105712.
DOI: 10.1038/s41467-023-37882-2.
P-Stereogenic Ir-MaxPHOX: A Step toward Privileged Catalysts for Asymmetric Hydrogenation of Nonchelating Olefins.
Biosca M, de la Cruz-Sanchez P, Faiges J, Margalef J, Salomo E, Riera A
ACS Catal. 2023; 13(5):3020-3035.
PMID: 36910869
PMC: 9990153.
DOI: 10.1021/acscatal.2c05579.
Structural analysis of an anthrol reductase inspires enantioselective synthesis of enantiopure hydroxycycloketones and β-halohydrins.
Hou X, Xu H, Yuan Z, Deng Z, Fu K, Gao Y
Nat Commun. 2023; 14(1):353.
PMID: 36681664
PMC: 9867772.
DOI: 10.1038/s41467-023-36064-4.
The Implications of the Brønsted Acidic Properties of Crabtree-Type Catalysts in the Asymmetric Hydrogenation of Olefins.
Peters B, Andersson P
J Am Chem Soc. 2022; 144(36):16252-16261.
PMID: 36044252
PMC: 9479089.
DOI: 10.1021/jacs.2c07023.
A Plausible Mechanism for the Iridium-Catalyzed Hydrogenation of a Bulky -Aryl Imine in the ()-Metolachlor Process.
Kwan A, Morris R
Molecules. 2022; 27(16).
PMID: 36014344
PMC: 9414898.
DOI: 10.3390/molecules27165106.
Nickel-catalysed asymmetric hydrogenation of oximes.
Li B, Chen J, Liu D, Gridnev I, Zhang W
Nat Chem. 2022; 14(8):920-927.
PMID: 35697929
DOI: 10.1038/s41557-022-00971-8.
Pd nanoparticles on green support as dip-catalyst: a facile transfer hydrogenation of olefins and -heteroarenes in water.
Shaikh M
RSC Adv. 2022; 9(48):28199-28206.
PMID: 35530451
PMC: 9071050.
DOI: 10.1039/c9ra06285h.
Efficient access to chiral dihydrobenzoxazinones Rh-catalyzed hydrogenation.
Chen Z, Yin X, Dong X, Zhang X
RSC Adv. 2022; 9(27):15466-15469.
PMID: 35514854
PMC: 9064260.
DOI: 10.1039/c9ra02694k.
Fullerene C promoted photochemical hydroamination reactions of an electron deficient alkyne with trimethylsilyl group containing tertiary -alkylbenzylamines.
Lim S, Jang H, Cho D
RSC Adv. 2022; 11(11):5914-5922.
PMID: 35423137
PMC: 8694821.
DOI: 10.1039/d1ra00166c.