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For: Hu Y, Chen J, Li B, Zhang Z, Gridnev ID, Zhang W. Nickel‐Catalyzed Asymmetric Hydrogenation of 2‐Amidoacrylates. Angew Chem Int Ed 2020;59:5371-5. [DOI: 10.1002/anie.201916534] [Cited by in Crossref: 27] [Cited by in F6Publishing: 38] [Article Influence: 13.5] [Reference Citation Analysis]
Number Citing Articles
1 Lu D, Li S, Yang X, Yin SF, Kambe N, Qiu R. Copper-Catalyzed Regioselective Olefination and Trifluoromethylation of Carboxylic Acids To Give (Z)-Trifluoromethyl Enol Esters. Org Lett 2022. [PMID: 35833663 DOI: 10.1021/acs.orglett.2c02027] [Reference Citation Analysis]
2 Chen Y, Yi X, Cheng Y, Huang A, Yang Z, Zhao X, Ling F, Zhong W. Rh-Catalyzed Highly Enantioselective Hydrogenation of Functionalized Olefins with Chiral Ferrocenylphosphine-Spiro Phosphonamidite Ligands. J Org Chem 2022;87:7864-74. [PMID: 35676758 DOI: 10.1021/acs.joc.2c00532] [Reference Citation Analysis]
3 Liu C, Wang M, Xu Y, Li Y, Liu Q. Manganese-Catalyzed Asymmetric Hydrogenation of 3H-Indoles. Angew Chem Int Ed Engl 2022;61:e202202814. [PMID: 35238455 DOI: 10.1002/anie.202202814] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Deng CQ, Liu J, Luo JH, Gan LJ, Deng J, Fu Y. Proton-Promoted Nickel-Catalyzed Asymmetric Hydrogenation of Aliphatic Ketoacids. Angew Chem Int Ed Engl 2022;61:e202115983. [PMID: 35099846 DOI: 10.1002/anie.202115983] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
5 Xiao G, Xie C, Guo Q, Zi G, Hou G, Huang Y. Nickel-Catalyzed Asymmetric Hydrogenation of γ-Keto Acids, Esters, and Amides to Chiral γ-Lactones and γ-Hydroxy Acid Derivatives. Org Lett 2022. [PMID: 35363497 DOI: 10.1021/acs.orglett.2c00826] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
6 Deng C, Liu J, Luo J, Gan L, Deng J, Fu Y. Proton‐Promoted Nickel‐Catalyzed Asymmetric Hydrogenation of Aliphatic Ketoacids. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202115983] [Reference Citation Analysis]
7 Xu M, Wang Y, Zhou Y, Yao Z. N,N-Chelate nickel(II) complexes bearing Schiff base ligands as efficient hydrogenation catalysts for amine synthesis. Journal of Organometallic Chemistry 2022;959:122187. [DOI: 10.1016/j.jorganchem.2021.122187] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Xiao G, Xie C, Guo Q, Zi G, Hou G, Huang Y. Highly enantioselective Ni-catalyzed asymmetric hydrogenation of β,β-disubstituted acrylic acids. Org Chem Front . [DOI: 10.1039/d2qo00652a] [Reference Citation Analysis]
9 Li M, Zhang J, Zou Y, Zhou F, Zhang Z, Zhang W. Asymmetric hydrogenation for the synthesis of 2-substituted chiral morpholines. Chem Sci 2021;12:15061-6. [PMID: 34909146 DOI: 10.1039/d1sc04288b] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Sen A, Chikkali SH. C 1-Symmetric diphosphorus ligands in metal-catalyzed asymmetric hydrogenation to prepare chiral compounds. Org Biomol Chem 2021;19:9095-137. [PMID: 34617539 DOI: 10.1039/d1ob01207j] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Zhou JS, Guo S, Zhao X, Chi YR. Nickel-catalyzed enantioselective umpolung hydrogenation for stereoselective synthesis of β-amido esters. Chem Commun (Camb) 2021;57:11501-4. [PMID: 34652359 DOI: 10.1039/d1cc05257h] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
12 Xu Y, Liu D, Deng Y, Zhou Y, Zhang W. Rhodium-Catalyzed Asymmetric Hydrogenation of 3-Benzoylaminocoumarins for the Synthesis of Chiral 3-Amino Dihydrocoumarins. Angew Chem Int Ed Engl 2021;60:23602-7. [PMID: 34596267 DOI: 10.1002/anie.202110286] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Cabré A, Verdaguer X, Riera A. Recent Advances in the Enantioselective Synthesis of Chiral Amines via Transition Metal-Catalyzed Asymmetric Hydrogenation. Chem Rev 2021. [PMID: 34677059 DOI: 10.1021/acs.chemrev.1c00496] [Cited by in F6Publishing: 21] [Reference Citation Analysis]
14 Zhao Y, Ding YX, Wu B, Zhou YG. Nickel-Catalyzed Asymmetric Hydrogenation for Kinetic Resolution of [2.2]Paracyclophane-Derived Cyclic N-Sulfonylimines. J Org Chem 2021;86:10788-98. [PMID: 34264081 DOI: 10.1021/acs.joc.1c01011] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
15 Zhang J, Chen T, Wang Y, Zhou F, Zhang Z, Gridnev ID, Zhang W. Asymmetric hydrogenation of γ ‐branched allylamines for the efficient synthesis of γ ‐chirogenic amines. Natural Sciences 2021;1. [DOI: 10.1002/ntls.10021] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
16 Hu Y, Zhang Z, Liu Y, Zhang W. Cobalt-Catalyzed Chemo- and Enantioselective Hydrogenation of Conjugated Enynes. Angew Chem Int Ed Engl 2021;60:16989-93. [PMID: 34062038 DOI: 10.1002/anie.202106566] [Cited by in F6Publishing: 12] [Reference Citation Analysis]
17 Hu Y, Zhang Z, Liu Y, Zhang W. Cobalt‐Catalyzed Chemo‐ and Enantioselective Hydrogenation of Conjugated Enynes. Angew Chem 2021;133:17126-30. [DOI: 10.1002/ange.202106566] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Li B, Liu D, Hu Y, Chen J, Zhang Z, Zhang W. Nickel‐Catalyzed Asymmetric Hydrogenation of Hydrazones. Eur J Org Chem 2021;2021:3421-5. [DOI: 10.1002/ejoc.202100642] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
19 Fan X, Zheng L, Yang Y, Dong X, Zhang X, Chung LW. A Computational Study of Asymmetric Hydrogenation of 2‐Phenyl Acrylic Acids Catalyzed by a Rh(I) Catalyst with Ferrocenyl Chiral Bisphosphorus Ligand: The Role of Ion‐Pair Interaction . Chin J Chem 2021;39:1616-24. [DOI: 10.1002/cjoc.202000741] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Xia J, Hirai T, Katayama S, Nagae H, Zhang W, Mashima K. Mechanistic Study of Ni and Cu Dual Catalyst for Asymmetric C–C Bond Formation; Asymmetric Coupling of 1,3-Dienes with C-nucleophiles to Construct Vicinal Stereocenters. ACS Catal 2021;11:6643-55. [DOI: 10.1021/acscatal.1c01626] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 16.0] [Reference Citation Analysis]
21 Parker PD, Hou X, Dong VM. Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis. J Am Chem Soc 2021;143:6724-45. [PMID: 33891819 DOI: 10.1021/jacs.1c00750] [Cited by in Crossref: 5] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
22 Dai Y, Chen J, Wang Z, Wang T, Wang L, Yang Y, Qiao X, Fan B. Asymmetric Reduction of Aromatic α-Dehydroamino Acid Esters with Water as Hydrogen Source. J Org Chem 2021;86:7141-7. [PMID: 33966384 DOI: 10.1021/acs.joc.1c00426] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Du X, Xiao Y, Yang Y, Duan Y, Li F, Hu Q, Chung LW, Chen G, Zhang X. Enantioselective Hydrogenation of Tetrasubstituted α,β‐Unsaturated Carboxylic Acids Enabled by Cobalt(II) Catalysis: Scope and Mechanistic Insights. Angew Chem 2021;133:11485-91. [DOI: 10.1002/ange.202016705] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
24 Du X, Xiao Y, Yang Y, Duan Y, Li F, Hu Q, Chung LW, Chen G, Zhang X. Enantioselective Hydrogenation of Tetrasubstituted α,β‐Unsaturated Carboxylic Acids Enabled by Cobalt(II) Catalysis: Scope and Mechanistic Insights. Angew Chem Int Ed 2021;60:11384-90. [DOI: 10.1002/anie.202016705] [Cited by in Crossref: 7] [Cited by in F6Publishing: 17] [Article Influence: 7.0] [Reference Citation Analysis]
25 Liu G, Tian K, Li C, You C, Tan X, Zhang H, Zhang X, Dong XQ. Nickel-Catalyzed Asymmetric Hydrogenation of Cyclic Alkenyl Sulfones, Benzo[b]thiophene 1,1-Dioxides, with Mechanistic Studies. Org Lett 2021;23:668-75. [PMID: 33471538 DOI: 10.1021/acs.orglett.0c03723] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
26 Liu C, Wang M, Liu S, Wang Y, Peng Y, Lan Y, Liu Q. Manganese‐Catalyzed Asymmetric Hydrogenation of Quinolines Enabled by π–π Interaction**. Angew Chem 2021;133:5168-73. [DOI: 10.1002/ange.202013540] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
27 Liu C, Wang M, Liu S, Wang Y, Peng Y, Lan Y, Liu Q. Manganese‐Catalyzed Asymmetric Hydrogenation of Quinolines Enabled by π–π Interaction**. Angew Chem Int Ed 2021;60:5108-13. [DOI: 10.1002/anie.202013540] [Cited by in Crossref: 11] [Cited by in F6Publishing: 32] [Article Influence: 11.0] [Reference Citation Analysis]
28 Wen J, Wang F, Zhang X. Asymmetric hydrogenation catalyzed by first-row transition metal complexes. Chem Soc Rev 2021;50:3211-37. [DOI: 10.1039/d0cs00082e] [Cited by in Crossref: 23] [Cited by in F6Publishing: 44] [Article Influence: 23.0] [Reference Citation Analysis]
29 Wu L, Wei H, Shen J, Chen J, Zhang W. Development of Earth-Abundant Metals-Catalyzed Enantioselective Alkenylations Using Alkenyl Metal Reagents. Acta Chimica Sinica 2021;79:1331. [DOI: 10.6023/a21070338] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Wu L, Wei H, Chen J, Zhang W. Development of Nickel-Catalyzed Cross-Coupling of Alcohol Derivatives to Construct Carbon-Carbon Bonds. Chinese Journal of Organic Chemistry 2021;41:4208. [DOI: 10.6023/cjoc202106021] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
31 Liu D, Li B, Chen J, Gridnev ID, Yan D, Zhang W. Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines. Nat Commun 2020;11:5935. [PMID: 33230219 DOI: 10.1038/s41467-020-19807-5] [Cited by in Crossref: 17] [Cited by in F6Publishing: 32] [Article Influence: 8.5] [Reference Citation Analysis]
32 Montes-Andrés H, Leo P, Muñoz A, Rodríguez-Diéguez A, Orcajo G, Choquesillo-Lazarte D, Martos C, Martínez F, Botas JA, Calleja G. Two Isostructural URJC-4 Materials: From Hydrogen Physisorption to Heterogeneous Reductive Amination through Hydrogen Molecule Activation at Low Pressure. Inorg Chem 2020;59:15733-40. [PMID: 33035421 DOI: 10.1021/acs.inorgchem.0c02127] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
33 Ponra S, Boudet B, Phansavath P, Ratovelomanana-vidal V. Recent Developments in Transition-Metal-Catalyzed Asymmetric Hydrogenation of Enamides. Synthesis 2020;53:193-214. [DOI: 10.1055/s-0040-1705939] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 5.5] [Reference Citation Analysis]
34 Lv B, Lei C, Ren F, Wang M, Hua F, Meng S, Yang Y, Yang Z, Lei Z. Asymmetric Hydrogenation of Acetophenone Catalyzed by Chirally Modified Ruthenium Nanoparticles Supported on Carbon Nanotubes. ChemistrySelect 2020;5:11803-10. [DOI: 10.1002/slct.202003232] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
35 Shen GB, Fu YH, Zhu XQ. Thermodynamic Network Cards of Hantzsch Ester, Benzothiazoline, and Dihydrophenanthridine Releasing Two Hydrogen Atoms or Ions on 20 Elementary Steps. J Org Chem 2020;85:12535-43. [PMID: 32880175 DOI: 10.1021/acs.joc.0c01726] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
36 Feng S, Tang Y, Yang C, Shen C, Dong K. Synthesis of Enantioenriched α,α-Difluoro-β-arylbutanoic Esters by Pd-Catalyzed Asymmetric Hydrogenation. Org Lett 2020;22:7508-12. [PMID: 32945684 DOI: 10.1021/acs.orglett.0c02700] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
37 Liu Y, Yi Z, Yang X, Wang H, Yin C, Wang M, Dong X, Zhang X. Efficient Access to Chiral 2-Oxazolidinones via Ni-Catalyzed Asymmetric Hydrogenation: Scope Study, Mechanistic Explanation, and Origin of Enantioselectivity. ACS Catal 2020;10:11153-61. [DOI: 10.1021/acscatal.0c02569] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 9.5] [Reference Citation Analysis]
38 Liu G, Zhang X, Wang H, Cong H, Zhang X, Dong XQ. Synthesis of chiral α-substituted α-amino acid and amine derivatives through Ni-catalyzed asymmetric hydrogenation. Chem Commun (Camb) 2020;56:4934-7. [PMID: 32239044 DOI: 10.1039/d0cc01220c] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]