Year |
Citation |
Score |
2023 |
Wang Y, He Y, Zhu S. Nickel-Catalyzed Migratory Cross-Coupling Reactions: New Opportunities for Selective C-H Functionalization. Accounts of Chemical Research. 56: 3475-3491. PMID 37971926 DOI: 10.1021/acs.accounts.3c00540 |
0.311 |
|
2023 |
Chen J, Wu L, Zhao Y, Zhu S. Enantio- and Diastereoselective NiH-Catalyzed Hydroalkylation of Enamides or Enecarbamates with Racemic α-Bromoamides. Angewandte Chemie (International Ed. in English). 62: e202311094. PMID 37721974 DOI: 10.1002/anie.202311094 |
0.505 |
|
2023 |
Chen C, Guo W, Qiao D, Zhu S. Synthesis of Enantioenriched 1,2-cis Disubstituted Cycloalkanes by Convergent NiH Catalysis. Angewandte Chemie (International Ed. in English). e202308320. PMID 37470299 DOI: 10.1002/anie.202308320 |
0.39 |
|
2023 |
Yang J, Gui Z, He Y, Zhu S. Functionalization of Olefinic C-H Bonds by an Aryl-to-Vinyl 1,4-Nickel Migration/Reductive Coupling Sequence. Angewandte Chemie (International Ed. in English). e202304713. PMID 37147743 DOI: 10.1002/anie.202304713 |
0.357 |
|
2022 |
Jiang X, Sheng FT, Zhang Y, Deng G, Zhu S. Ligand Relay Catalysis Enables Asymmetric Migratory Reductive Acylation of Olefins or Alkyl Halides. Journal of the American Chemical Society. PMID 36395247 DOI: 10.1021/jacs.2c10785 |
0.431 |
|
2022 |
Wang Y, He Y, Zhu S. NiH-Catalyzed Functionalization of Remote and Proximal Olefins: New Reactions and Innovative Strategies. Accounts of Chemical Research. 55: 3519-3536. PMID 36350093 DOI: 10.1021/acs.accounts.2c00628 |
0.416 |
|
2022 |
Zhang Y, Qiao D, Duan M, Wang Y, Zhu S. Enantioselective synthesis of α-aminoboronates by NiH-catalysed asymmetric hydroamidation of alkenyl boronates. Nature Communications. 13: 5630. PMID 36163363 DOI: 10.1038/s41467-022-33411-9 |
0.487 |
|
2022 |
He Y, Ma J, Song H, Zhang Y, Liang Y, Wang Y, Zhu S. Regio- and enantioselective remote hydroarylation using a ligand-relay strategy. Nature Communications. 13: 2471. PMID 35513385 DOI: 10.1038/s41467-022-30006-2 |
0.368 |
|
2021 |
He Y, Börjesson M, Song H, Xue Y, Zeng D, Martin R, Zhu S. Nickel-Catalyzed Difunctionalization of Aryl Bromides with Alkynes and Alkyl Bromides via a Vinyl-to-Aryl 1,4-Hydride Shift. Journal of the American Chemical Society. PMID 34793680 DOI: 10.1021/jacs.1c10368 |
0.638 |
|
2021 |
Meng L, Yang J, Duan M, Wang Y, Zhu S. Facile Synthesis of Chiral Arylamines, Alkylamines and Amides by Enantioselective NiH-Catalyzed Hydroamination. Angewandte Chemie (International Ed. in English). PMID 34449971 DOI: 10.1002/anie.202109881 |
0.526 |
|
2021 |
Chen J, Zhu S. Nickel-Catalyzed Multicomponent Coupling: Synthesis of α-Chiral Ketones by Reductive Hydrocarbonylation of Alkenes. Journal of the American Chemical Society. PMID 34436887 DOI: 10.1021/jacs.1c07851 |
0.478 |
|
2021 |
Jiang X, Han B, Xue Y, Duan M, Gui Z, Wang Y, Zhu S. Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. Nature Communications. 12: 3792. PMID 34145283 DOI: 10.1038/s41467-021-24094-9 |
0.511 |
|
2021 |
Jiang X, Han B, Xue Y, Duan M, Gui Z, Wang Y, Zhu S. Nickel-catalysed migratory hydroalkynylation and enantioselective hydroalkynylation of olefins with bromoalkynes. Nature Communications. 12: 3792. PMID 34145283 DOI: 10.1038/s41467-021-24094-9 |
0.511 |
|
2021 |
He Y, Song H, Chen J, Zhu S. NiH-catalyzed asymmetric hydroarylation of N-acyl enamines to chiral benzylamines. Nature Communications. 12: 638. PMID 33504793 DOI: 10.1038/s41467-020-20888-5 |
0.441 |
|
2020 |
Liu J, Gong H, Zhu S. Nickel-Catalyzed, Regio- and Enantioselective Benzylic Alkenylation of Olefins with Alkenyl Bromide. Angewandte Chemie (International Ed. in English). PMID 33171012 DOI: 10.1002/anie.202012614 |
0.501 |
|
2020 |
He Y, Liu C, Yu L, Zhu S. Enantio- and Regioselective NiH-Catalyzed Reductive Hydroarylation of Vinylarenes with Aryl Iodides. Angewandte Chemie (International Ed. in English). PMID 32805082 DOI: 10.1002/Anie.202010386 |
0.519 |
|
2020 |
He Y, Liu C, Yu L, Zhu S. Ligand-Enabled Nickel-Catalyzed Redox-Relay Migratory Hydroarylation of Alkenes with Arylborons. Angewandte Chemie (International Ed. in English). PMID 32141689 DOI: 10.1002/Anie.202001742 |
0.501 |
|
2020 |
Chen F, Xu X, He Y, Huang G, Zhu S. NiH-Catalyzed Migratory Defluorinative Cross Olefin-Coupling: Trifluoromethyl-Substituted Alkenes as Acceptor Olefins to Form gem-Difluoroalkenes. Angewandte Chemie (International Ed. in English). PMID 31951070 DOI: 10.1002/Anie.201915840 |
0.428 |
|
2019 |
He J, Xue Y, Han B, Zhang C, Wang Y, Zhu S. Nickel-Catalyzed Asymmetric Reductive 1,2-Carboamination of Unactivated Alkenes. Angewandte Chemie (International Ed. in English). PMID 31755199 DOI: 10.1002/Anie.201913743 |
0.593 |
|
2019 |
Zhang Y, Han B, Zhu S. Rapid Access to Highly Functionalized Alkylboronates via NiH-Catalyzed Remote Hydroarylation of Boron-Containing Alkenes. Angewandte Chemie (International Ed. in English). PMID 31287597 DOI: 10.1002/Anie.201907185 |
0.496 |
|
2019 |
Zhang Y, Xu X, Zhu S. Nickel-catalysed selective migratory hydrothiolation of alkenes and alkynes with thiols. Nature Communications. 10: 1752. PMID 30988306 DOI: 10.1038/S41467-019-09783-W |
0.485 |
|
2019 |
He J, Song P, Xu X, Zhu S, Wang Y. Migratory Reductive Acylation between Alkyl Halides or Alkenes and Alkyl Carboxylic Acids by Nickel Catalysis Acs Catalysis. 9: 3253-3259. DOI: 10.1021/Acscatal.9B00521 |
0.52 |
|
2018 |
Zhou F, Zhang Y, Xu X, Zhu S. NiH-Catalyzed Asymmetric Remote Hydroalkylation of Alkenes with Racemic α-Bromo Amides. Angewandte Chemie (International Ed. in English). PMID 30548518 DOI: 10.1002/Anie.201813222 |
0.543 |
|
2018 |
Ichikawa S, Zhu S, Buchwald SL. A Modified System for the Synthesis of Enantioenriched N-Arylamines through Copper-Catalyzed Hydroamination. Angewandte Chemie (International Ed. in English). PMID 29847002 DOI: 10.1002/Anie.201803026 |
0.654 |
|
2018 |
Zhou F, Zhu J, Zhang Y, Zhu S. NiH-Catalyzed Reductive Relay Hydroalkylation: A Strategy for Remote sp3 C-H Alkylation of Alkenes. Angewandte Chemie (International Ed. in English). PMID 29460343 DOI: 10.1002/Anie.201712731 |
0.415 |
|
2018 |
Xiao J, He Y, Ye F, Zhu S. Remote sp3 C–H Amination of Alkenes with Nitroarenes Chem. 4: 1645-1657. DOI: 10.1016/J.Chempr.2018.04.008 |
0.482 |
|
2017 |
Chen F, Chen K, Zhang Y, He Y, Wang YM, Zhu S. Remote Migratory Cross-Electrophile Coupling and Olefin Hydroarylation Reactions Enabled by in situ Generation of NiH. Journal of the American Chemical Society. PMID 28880544 DOI: 10.1021/Jacs.7B08064 |
0.604 |
|
2017 |
Chen F, Zhang Y, Yu L, Zhu S. Enantioselective NiH/Pmrox-Catalyzed 1,2-Reduction of α,β-Unsaturated Ketones. Angewandte Chemie (International Ed. in English). PMID 28090717 DOI: 10.1002/Anie.201610990 |
0.536 |
|
2017 |
He Y, Cai Y, Zhu S. Mild and Regioselective Benzylic C-H Functionalization: Ni-Catalyzed Reductive Arylation of Remote and Proximal Olefins. Journal of the American Chemical Society. PMID 28051861 DOI: 10.1021/Jacs.6B11962 |
0.571 |
|
2016 |
Zhu S, Niljianskul N, Buchwald SL. A direct approach to amines with remote stereocentres by enantioselective CuH-catalysed reductive relay hydroamination. Nature Chemistry. 8: 144-50. PMID 26791897 DOI: 10.1038/Nchem.2418 |
0.759 |
|
2015 |
Wang YM, Bruno NC, Placeres ÁL, Zhu S, Buchwald SL. Enantioselective Synthesis of Carbo- and Heterocycles through a CuH-Catalyzed Hydroalkylation Approach. Journal of the American Chemical Society. 137: 10524-7. PMID 26256576 DOI: 10.1021/Jacs.5B07061 |
0.757 |
|
2015 |
Niljianskul N, Zhu S, Buchwald SL. Enantioselective synthesis of α-aminosilanes by copper-catalyzed hydroamination of vinylsilanes. Angewandte Chemie (International Ed. in English). 54: 1638-41. PMID 25475991 DOI: 10.1002/Anie.201410326 |
0.779 |
|
2014 |
Zhu S, Buchwald SL. Enantioselective CuH-catalyzed anti-Markovnikov hydroamination of 1,1-disubstituted alkenes. Journal of the American Chemical Society. 136: 15913-6. PMID 25339089 DOI: 10.1021/Ja509786V |
0.677 |
|
2013 |
Evans RW, Zbieg JR, Zhu S, Li W, MacMillan DW. Simple catalytic mechanism for the direct coupling of α-carbonyls with functionalized amines: a one-step synthesis of Plavix. Journal of the American Chemical Society. 135: 16074-7. PMID 24107144 DOI: 10.1021/Ja4096472 |
0.752 |
|
2013 |
Zhu S, Niljianskul N, Buchwald SL. Enantio- and regioselective CuH-catalyzed hydroamination of alkenes. Journal of the American Chemical Society. 135: 15746-9. PMID 24106781 DOI: 10.1021/Ja4092819 |
0.768 |
|
2012 |
Zhu S, MacMillan DW. Enantioselective copper-catalyzed construction of aryl pyrroloindolines via an arylation-cyclization cascade. Journal of the American Chemical Society. 134: 10815-8. PMID 22716914 DOI: 10.1021/Ja305100G |
0.734 |
|
2011 |
Wang Y, Zhu S, Ma D. Organocatalytic approach to polysubstituted piperidines and tetrahydropyrans. Organic Letters. 13: 1602-5. PMID 21361355 DOI: 10.1021/Ol200004S |
0.642 |
|
2011 |
Yu S, Zhu S, Pan X, Yang J, Ma D. Reinvestigation on total synthesis of kaitocephalin and its isomers Tetrahedron. 67: 1673-1680. DOI: 10.1016/J.Tet.2010.12.068 |
0.732 |
|
2010 |
Zhu S, Yu S, Wang Y, Ma D. Organocatalytic Michael addition of aldehydes to protected 2-amino-1-nitroethenes: the practical syntheses of oseltamivir (Tamiflu) and substituted 3-aminopyrrolidines. Angewandte Chemie (International Ed. in English). 49: 4656-60. PMID 20480479 DOI: 10.1002/Anie.201001644 |
0.704 |
|
2009 |
Zhu S, Wang Y, Ma D. Enantioselective Organocatalytic Conjugate Addition of Aldehydes to α,β-Unsaturated Thiol Esters Advanced Synthesis & Catalysis. 351: 2563-2566. DOI: 10.1002/Adsc.200900449 |
0.658 |
|
2008 |
Zhu S, Yu S, Ma D. Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water. Angewandte Chemie (International Ed. in English). 47: 545-8. PMID 18038442 DOI: 10.1002/Anie.200704161 |
0.695 |
|
2008 |
Ma A, Zhu S, Ma D. Enantioselective organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in water Tetrahedron Letters. 49: 3075-3077. DOI: 10.1016/J.Tetlet.2008.03.051 |
0.605 |
|
Low-probability matches (unlikely to be authored by this person) |
2017 |
He Y, Cai Y, Zhu S. Addition to "Mild and Regioselective Benzylic C-H Functionalization: Ni-Catalyzed Reductive Arylation of Remote and Proximal Olefins". Journal of the American Chemical Society. PMID 28139920 DOI: 10.1021/jacs.7b00683 |
0.294 |
|
2016 |
Chen YW, Li B, Niu Q, Li L, Kan JW, Zhu SM, Shen SB. Combined promoting effects of low-Pd-containing and Cu-doped LaCoO3 perovskite supported on cordierite for the catalytic combustion of benzene. Environmental Science and Pollution Research International. PMID 27094280 DOI: 10.1007/s11356-016-6594-4 |
0.228 |
|
2024 |
Zhou J, He Y, Liu Z, Wang Y, Zhu S. Ligand Relay Catalysis Enables Asymmetric Migratory Hydroarylation for the Concise Synthesis of Chiral α-(Hetero)Aryl-Substituted Amines. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2306447. PMID 38419384 DOI: 10.1002/advs.202306447 |
0.12 |
|
2021 |
Mi C, Zhu S, Nie R. Improving Loanword Identification in Low-Resource Language with Data Augmentation and Multiple Feature Fusion. Computational Intelligence and Neuroscience. 2021: 9975078. PMID 33927756 DOI: 10.1155/2021/9975078 |
0.034 |
|
2012 |
Gong G, Yang Z, Zhu S. Numerical investigation of the effect of helix angle and leaf margin on the flow pattern and the performance of the axial flow cyclone separator Applied Mathematical Modelling. 36: 3916-3930. DOI: 10.1016/j.apm.2011.11.034 |
0.022 |
|
2007 |
Du G, Yang HY, Zhu SL, Zhang GQ. [Experiment on seeding induction from seed of Demdrobium candidum]. Zhong Yao Cai = Zhongyaocai = Journal of Chinese Medicinal Materials. 30: 1207-8. PMID 18300485 |
0.014 |
|
2020 |
Zhu S, Yang Y, Xu C. Extracting Parallel Sentences from Nonparallel Corpora Using Parallel Hierarchical Attention Network. Computational Intelligence and Neuroscience. 2020: 8823906. PMID 32952544 DOI: 10.1155/2020/8823906 |
0.01 |
|
Hide low-probability matches. |