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Shaolin Zhu - Publications

Affiliations: 
Nanjing University, Nanjing Shi, Jiangsu Sheng, China 
Website:
http://chem.nju.edu.cn/staff/staff.asp?iname=%D6%EC%C9%D9%C1%D6

42 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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
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