Xie JB - Search Results

1

Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: enantioselective total synthesis of (-)-mesembrine.

Zhang QQ, Xie JH, Yang XH, Xie JB, Zhou QL. Zhang QQ, et al. Among authors: xie jh, xie jb. Org Lett. 2012 Dec 21;14(24):6158-61. doi: 10.1021/ol302842h. Epub 2012 Dec 4. Org Lett. 2012. PMID: 23210605

2

Well-defined chiral spiro iridium/phosphine-oxazoline cationic complexes for highly enantioselective hydrogenation of imines at ambient pressure.

Zhu SF, Xie JB, Zhang YZ, Li S, Zhou QL. Zhu SF, et al. Among authors: xie jb. J Am Chem Soc. 2006 Oct 4;128(39):12886-91. doi: 10.1021/ja063444p. J Am Chem Soc. 2006. PMID: 17002383

3

Highly enantioselective hydrogenation of alpha-arylmethylene cycloalkanones catalyzed by iridium complexes of chiral spiro aminophosphine ligands.

Xie JB, Xie JH, Liu XY, Kong WL, Li S, Zhou QL. Xie JB, et al. Among authors: xie jh. J Am Chem Soc. 2010 Apr 7;132(13):4538-9. doi: 10.1021/ja100652f. J Am Chem Soc. 2010. PMID: 20232874

4

Chiral iridium spiro aminophosphine complexes: asymmetric hydrogenation of simple ketones, structure, and plausible mechanism.

Xie JB, Xie JH, Liu XY, Zhang QQ, Zhou QL. Xie JB, et al. Among authors: xie jh. Chem Asian J. 2011 Mar 1;6(3):899-908. doi: 10.1002/asia.201000716. Epub 2010 Dec 15. Chem Asian J. 2011. PMID: 21344665

5

An additional coordination group leads to extremely efficient chiral iridium catalysts for asymmetric hydrogenation of ketones.

Xie JH, Liu XY, Xie JB, Wang LX, Zhou QL. Xie JH, et al. Among authors: xie jb. Angew Chem Int Ed Engl. 2011 Aug 1;50(32):7329-32. doi: 10.1002/anie.201102710. Epub 2011 Jul 12. Angew Chem Int Ed Engl. 2011. PMID: 21751315 No abstract available.

6

Chiral iridium catalysts bearing spiro pyridine-aminophosphine ligands enable highly efficient asymmetric hydrogenation of β-aryl β-ketoesters.

Xie JH, Liu XY, Yang XH, Xie JB, Wang LX, Zhou QL. Xie JH, et al. Among authors: xie jb. Angew Chem Int Ed Engl. 2012 Jan 2;51(1):201-3. doi: 10.1002/anie.201105780. Epub 2011 Nov 16. Angew Chem Int Ed Engl. 2012. PMID: 22095722 No abstract available.

7

Asymmetric Catalytic Enantio- and Diastereoselective Boron Conjugate Addition Reactions of α-Functionalized α,β-Unsaturated Carbonyl Substrates.

Xie JB, Lin S, Qiao S, Li G. Xie JB, et al. Org Lett. 2016 Aug 5;18(15):3926-9. doi: 10.1021/acs.orglett.6b01998. Epub 2016 Jul 19. Org Lett. 2016. PMID: 27434500

8

Rhodium-Catalyzed Ring Expansion of Azetidines via Domino Conjugate Addition/N-Directed α-C(sp³)-H Activation.

Sun LZ, Yang X, Li NN, Li M, Ouyang Q, Xie JB. Sun LZ, et al. Among authors: xie jb. Org Lett. 2022 Mar 18;24(10):1883-1888. doi: 10.1021/acs.orglett.2c00056. Epub 2022 Mar 10. Org Lett. 2022. PMID: 35266389

9

Revisiting the Mg/TMSCl/Dipolar Solvent System for Dearomatic Silylation of Aryl Carbonyl Compounds: Substrate Scope, Transformations, and Mechanistic Studies.

Li NN, Li M, Gao JN, Zhang Z, Xie JB. Li NN, et al. Among authors: xie jb. J Org Chem. 2022 Aug 19;87(16):10876-10889. doi: 10.1021/acs.joc.2c01178. Epub 2022 Jul 29. J Org Chem. 2022. PMID: 35905447

10

Enantio- and diastereoselective boron conjugate addition to α-alkyl α,β-unsaturated esters.

Li M, Peng GR, Yang X, Ma ZN, Xie JB. Li M, et al. Among authors: xie jb. Org Biomol Chem. 2022 Dec 21;21(1):53-58. doi: 10.1039/d2ob01928k. Org Biomol Chem. 2022. PMID: 36468637

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