朱少林课题组

Nanjing University

School of Chemistry & Chemical Engineering

PUBLICATIONS

2020

Angew. Chem. Int. Ed. 2020, 59, 9186–9191.

12. Ligand-Enabled Nickel-Catalyzed Redox-Relay Migratory Hydroarylation of Alkenes with Arylborons.

Y. He, C. Liu, L. Yu, S. Zhu.

ACIE-2020-59-9186.pdf

Angew. Chem. Int. Ed. 2020, 59, 9186–9191.

12. Ligand-Enabled Nickel-Catalyzed Redox-Relay Migratory Hydroarylation of Alkenes with Arylborons.

Y. He, C. Liu, L. Yu, S. Zhu.

ACIE-2020-59-9186.pdf

Angew. Chem. Int. Ed. 2020, 59, 5398–5402.

11. NiH‐Catalyzed Migratory Defluorinative Olefin Cross‐Coupling: Trifluoromethyl‐Substituted Alkenes as Acceptor Olefins to Form gem‐Difluoroalkenes.

F. Chen, X. Xu, Y. He, G. Huang, S. Zhu.

ACIE-2020-59-5398.pdf

Angew. Chem. Int. Ed. 2020, 59, 2328–2332.

10. Nickel‐Catalyzed Asymmetric Reductive 1,2‐Carboamination of Unactivated Alkenes.

J. He, Y. Xue, B. Han, C. Zhang, Y. Wang, S. Zhu.

ACIE-2020-59-2328.pdf

2019

Angew. Chem. Int. Ed. 2019, 58, 13860–13864.

9. Rapid Access to Highly Functionalized Alkylboronates via NiH-Catalyzed Remote Hydroarylation of Boron-Containing Alkenes.

Y. Zhang, B. Han, S. Zhu.

ACIE-2019-58-13860.pdf

Nat. Commun. 2019, 10, 1752.

8. Nickel-Catalysed Selective Migratory Hydrothiolation of Alkenes and Alkynes with Thiols.

Y. Zhang, X. Xu, S. Zhu.

NC-2019-10-1752.pdf

ACS. Catal. 2019, 9, 3253–3259.

7. Migratory Reductive Acylation between Alkyl Halides or Alkenes and Alkyl Carboxylic Acids by Nickel Catalysis.

J. He, P. Song, X. Xu, S. Zhu, Y. Wang.

acscatal-2019-9-3253.pdf

Angew. Chem. Int. Ed. 2019, 58, 1754–1758.

6. NiH-Catalyzed Remote Asymmetric Hydroalkylation of Alkenes with Racemic α-Bromo Amides.

F. Zhou, Y. Zhang, X. Xu, S. Zhu.

ACIE-2019-58-1754.pdf

2018

Chem 2018, 4, 1645–1657.

5. Remote sp3 C–H Amination of Alkenes with Nitroarenes.

J. Xiao, Y. He, F. Ye, S. Zhu.

Chem-2018-4-16451657.pdf

Angew. Chem. Int. Ed. 2018, 57, 4058–4062.

4. NiH-Catalyzed Reductive Relay Hydroalkylation: A Strategy for the Remote C(sp3)–H Alkylation of Alkenes.

F. Zhou, J. Zhu, Y. Zhang, S. Zhu.

ACIE-2018-57-4058.pdf

2017

J. Am. Chem. Soc. 2017, 139, 13929–13935.

3. Remote Migratory Cross-Electrophile Coupling and Olefin Hydroarylation Reactions Enabled by in Situ Generation of NiH.

F. Chen, K. Chen, Y. Zhang, Y. He, Y.-M. Wang, S. Zhu.

JACS-2017-139-13929.pdf

J. Am. Chem. Soc. 2017, 139, 1061–1064.

2. Mild and Regioselective Benzylic C−H Functionalization: Ni-Catalyzed Reductive Arylation of Remote and Proximal Olefins.

Y. He, Y. Cai, S. Zhu.

JACS-2017-139-1061.pdf

Angew. Chem. Int. Ed. 2017, 56, 2022–2025.

1. Enantioselective NiH/Pmrox-Catalyzed 1,2-Reduction of α, β-Unsaturated Ketones.

F. Chen, Y. Zhang, L. Yu, S. Zhu.

ACIE-2017-56-2022.pdf

Pre-NJU Publications

14. A Modified System for the Synthesis of Enantioenriched N‐Arylamines through Copper‐Catalyzed Hydroamination.

S. Ichikawa, S. Zhu, S.L. Buchwald. Angew. Chem. Int. Ed. 2018, 57, 8714–8718.

13. A Direct Approach to Amines with Remote Stereocentres by Enantioselective CuH-catalysed Reductive Relay Hydroamination.

S. Zhu, N. Niljianskul, S. L. Buchwald. Nat. Chem. 2016, 8, 144–150.

12. Enantioselective Synthesis of Carbo- and Heterocycles through a CuH-Catalyzed Hydroalkylation Approach.

Y.-M. Wang, N. C. Bruno, Á. L. Placeres, S. Zhu, S. L. Buchwald. J. Am. Chem. Soc. 2015, 137, 10524–10527.

11. Enantioselective Synthesis of α-Aminosilanes by Copper-Catalyzed Hydroamination of Vinylsilanes.

N. Niljianskul, S. Zhu, S. L. Buchwald. Angew. Chem. Int. Ed. 2015, 54, 1638–1641.

10. Enantioselective CuH-Catalyzed Anti-Markovnikov Hydroamination of 1,1-Disubstituted Alkenes.

S. Zhu, S. L. Buchwald. J. Am. Chem. Soc. 2014, 136, 45, 15913–15916.

9. Enantio- and Regioselective CuH-Catalyzed Hydroamination of Alkenes.

S. Zhu, N. Niljianskul, S. L. Buchwald. J. Am. Chem. Soc. 2013, 135, 15746–15749.

8. A Simple Catalytic Mechanism for the Direct Coupling of α-Carbonyls with Functionalized Amines: A One-Step Synthesis of Plavix.

R. W. Evans, J.R. Zbieg, S. Zhu, W. Li, D. W. C. MacMillan. J. Am. Chem. Soc. 2013, 135, 16074–16077.

7. Enantioselective Copper-Catalyzed Construction of Aryl Pyrroloindolines via an Arylation-Cyclization Cascade.

S. Zhu, D. W. C. MacMillan. J. Am. Chem. Soc. 2012, 134, 10815–10818.

6. Organocatalytic Approach to Polysubstituted Piperidines and Tetrahydropyrans.

Y. Wang, S. Zhu, D. Ma. Org. Lett. 2011, 13, 1602–1605.

5. Reinvestigation on Total Synthesis of Kaitocephalin and its Isomers.

S. Yu, S. Zhu, X. Pan, J. Yang, D. Ma. Tetrahedron 2011, 67, 1673–1680.

4.Organocatalytic Michael Addition of Aldehydes to Protected 2-Amino-1-Nitroethenes: The Practical Syntheses of Oseltamivir (Tamiflu) and Substituted 3-Aminopyrrolidines.

S. Zhu, S. Yu, Y. Wang, D. Ma. Angew. Chem. Int. Ed. 2010, 49, 4656–4660.

3. Enantioselective Organocatalytic Conjugate Addition of Aldehydes to α,β-Unsaturated Thiol Esters.

S. Zhu, Y. Wang, D. Ma. Adv. Synth. Catal. 2009, 351, 2563–2566.

2. Enantioselective Organocatalytic Michael Addition of Malonates to α,β-Unsaturated Aldehydes in Water.

A. Ma, S. Zhu, D. Ma. Angew. Chem. Int. Ed. 2008, 47, 545–548.

1. Highly Efficient Catalytic System for Enantioselective Michael Addition of Aldehydes to Nitroalkenes in Water.

S. Zhu, S. Yu, D. Ma. Angew. Chem. Int. Ed. 2008, 47, 545–548