Zhang H - Search Results

1

Labile Cu(I) catalyst/spectator Cu(II) species in copper-catalyzed C-C coupling reaction: operando IR, in situ XANES/EXAFS evidence and kinetic investigations.

He C, Zhang G, Ke J, Zhang H, Miller JT, Kropf AJ, Lei A. He C, et al. Among authors: zhang g, zhang h. J Am Chem Soc. 2013 Jan 9;135(1):488-93. doi: 10.1021/ja310111p. Epub 2012 Dec 19. J Am Chem Soc. 2013. PMID: 23214954

2

Investigation of an efficient palladium-catalyzed C(sp)-C(sp) cross-coupling reaction using phosphine-olefin ligand: application and mechanistic aspects.

Shi W, Luo Y, Luo X, Chao L, Zhang H, Wang J, Lei A. Shi W, et al. Among authors: zhang h. J Am Chem Soc. 2008 Nov 5;130(44):14713-20. doi: 10.1021/ja8049436. Epub 2008 Oct 11. J Am Chem Soc. 2008. PMID: 18847269

3

Direct observation of reduction of Cu(II) to Cu(I) by terminal alkynes.

Zhang G, Yi H, Zhang G, Deng Y, Bai R, Zhang H, Miller JT, Kropf AJ, Bunel EE, Lei A. Zhang G, et al. Among authors: zhang h. J Am Chem Soc. 2014 Jan 22;136(3):924-6. doi: 10.1021/ja410756b. Epub 2014 Jan 10. J Am Chem Soc. 2014. PMID: 24392805

4

Oxidative cross-coupling through double transmetallation: surprisingly high selectivity for palladium-catalyzed cross-coupling of alkylzinc and alkynylstannanes.

Zhao Y, Wang H, Hou X, Hu Y, Lei A, Zhang H, Zhu L. Zhao Y, et al. Among authors: zhang h. J Am Chem Soc. 2006 Nov 29;128(47):15048-9. doi: 10.1021/ja0647351. J Am Chem Soc. 2006. PMID: 17117830

5

Base-induced mechanistic variation in palladium-catalyzed carbonylation of aryl iodides.

Hu Y, Liu J, Lü Z, Luo X, Zhang H, Lan Y, Lei A. Hu Y, et al. Among authors: zhang h. J Am Chem Soc. 2010 Mar 10;132(9):3153-8. doi: 10.1021/ja909962f. J Am Chem Soc. 2010. PMID: 20143770

6

Organocatalysis in cross-coupling: DMEDA-catalyzed direct C-H arylation of unactivated benzene.

Liu W, Cao H, Zhang H, Zhang H, Chung KH, He C, Wang H, Kwong FY, Lei A. Liu W, et al. Among authors: zhang h. J Am Chem Soc. 2010 Dec 1;132(47):16737-40. doi: 10.1021/ja103050x. Epub 2010 Aug 2. J Am Chem Soc. 2010. PMID: 20677824

7

Which one is faster? A kinetic investigation of Pd and Ni catalyzed Negishi-type oxidative coupling reactions.

Xin J, Zhang G, Deng Y, Zhang H, Lei A. Xin J, et al. Among authors: zhang g, zhang h. Dalton Trans. 2015 Dec 14;44(46):19777-81. doi: 10.1039/c5dt03386a. Dalton Trans. 2015. PMID: 26536236

8

Electrochemical Oxidation Enables Regioselective and Scalable α-C(sp³)-H Acyloxylation of Sulfides.

Wang H, He M, Li Y, Zhang H, Yang D, Nagasaka M, Lv Z, Guan Z, Cao Y, Gong F, Zhou Z, Zhu J, Samanta S, Chowdhury AD, Lei A. Wang H, et al. Among authors: zhang h. J Am Chem Soc. 2021 Mar 10;143(9):3628-3637. doi: 10.1021/jacs.1c00288. Epub 2021 Feb 26. J Am Chem Soc. 2021. PMID: 33635055

9

Electrophotochemical Ce-Catalyzed Ring-Opening Functionalization of Cycloalkanols under Redox-Neutral Conditions: Scope and Mechanism.

Yang Z, Yang D, Zhang J, Tan C, Li J, Wang S, Zhang H, Huang Z, Lei A. Yang Z, et al. Among authors: zhang j, zhang h. J Am Chem Soc. 2022 Aug 3;144(30):13895-13902. doi: 10.1021/jacs.2c05520. Epub 2022 Jul 21. J Am Chem Soc. 2022. PMID: 35861667

10

Nickel-catalyzed oxidative coupling reactions of two different terminal alkynes using O(2) as the oxidant at room temperature: facile syntheses of unsymmetric 1,3-diynes.

Yin W, He C, Chen M, Zhang H, Lei A. Yin W, et al. Among authors: zhang h. Org Lett. 2009 Feb 5;11(3):709-12. doi: 10.1021/ol8027863. Org Lett. 2009. PMID: 19108674

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