Xu XY - Search Results

1

Asymmetric Michael/cyclization tandem reaction of 4-hydroxycoumarin with β-nitroalkenes catalyzed by chiral bifunctional thioureas.

Mei RQ, Xu XY, Peng L, Wang F, Tian F, Wang LX. Mei RQ, et al. Among authors: xu xy. Org Biomol Chem. 2013 Feb 28;11(8):1286-9. doi: 10.1039/c2ob27121d. Org Biomol Chem. 2013. PMID: 23338479

2

Highly enantioselective aldol reaction of acetone with β,γ-unsaturated α-keto esters promoted by simple chiral primary-tertiary diamine catalysts.

Peng L, Wang LL, Bai JF, Jia LN, Guo YL, Luo XY, Wang FY, Xu XY, Wang LX. Peng L, et al. Among authors: xu xy. Org Biomol Chem. 2011 Jul 7;9(13):4774-7. doi: 10.1039/c1ob05607g. Epub 2011 May 26. Org Biomol Chem. 2011. PMID: 21614388

3

Asymmetric hydroxyamination of oxindoles catalyzed by chiral bifunctional tertiary amine thiourea: construction of 3-amino-2-oxindoles with quaternary stereocenters.

Jia LN, Huang J, Peng L, Wang LL, Bai JF, Tian F, He GY, Xu XY, Wang LX. Jia LN, et al. Among authors: xu xy. Org Biomol Chem. 2012 Jan 14;10(2):236-9. doi: 10.1039/c1ob06413d. Epub 2011 Oct 21. Org Biomol Chem. 2012. PMID: 22016069

4

Asymmetric Michael addition of α-substituted isocyanoacetates with maleimides catalyzed by chiral tertiary amine thiourea.

Bai JF, Wang LL, Peng L, Guo YL, Jia LN, Tian F, He GY, Xu XY, Wang LX. Bai JF, et al. Among authors: xu xy. J Org Chem. 2012 Mar 16;77(6):2947-53. doi: 10.1021/jo2025288. Epub 2012 Mar 7. J Org Chem. 2012. PMID: 22369654

5

Direct asymmetric vinylogous Mannich reaction of 3,4-dihalofuran-2(5H)-one with aldimine catalyzed by quinine.

Guo YL, Bai JF, Peng L, Wang LL, Jia LN, Luo XY, Tian F, Xu XY, Wang LX. Guo YL, et al. Among authors: xu xy. J Org Chem. 2012 Sep 21;77(18):8338-43. doi: 10.1021/jo301115t. Epub 2012 Sep 10. J Org Chem. 2012. PMID: 22900985

6

An organocatalytic asymmetric sequential allylic alkylation-cyclization of Morita-Baylis-Hillman carbonates and 3-hydroxyoxindoles.

Wang QL, Peng L, Wang FY, Zhang ML, Jia LN, Tian F, Xu XY, Wang LX. Wang QL, et al. Among authors: xu xy. Chem Commun (Camb). 2013 Oct 21;49(82):9422-4. doi: 10.1039/c3cc45139a. Chem Commun (Camb). 2013. PMID: 24005475

7

An organocatalytic domino Michael-alkylation reaction: highly enantioselective construction of spiro-cyclopentanoneoxindoles and tetronic acid scaffolds.

Zhou J, Wang QL, Peng L, Tian F, Xu XY, Wang LX. Zhou J, et al. Among authors: xu xy. Chem Commun (Camb). 2014 Dec 4;50(93):14601-4. doi: 10.1039/c4cc05207b. Chem Commun (Camb). 2014. PMID: 25307364

8

Effective construction of quaternary stereocenters by highly enantioselective α-amination of branched aldehydes.

Fu JY, Xu XY, Li YC, Huang QC, Wang LX. Fu JY, et al. Among authors: xu xy. Org Biomol Chem. 2010 Oct 21;8(20):4524-6. doi: 10.1039/c0ob00406e. Epub 2010 Aug 23. Org Biomol Chem. 2010. PMID: 20733976

9

Highly organocatalytic asymmetric Michael-ketone aldol-dehydration domino reaction: straightforward approach to construct six-membered spirocyclic oxindoles.

Wang LL, Peng L, Bai JF, Huang QC, Xu XY, Wang LX. Wang LL, et al. Among authors: xu xy. Chem Commun (Camb). 2010 Nov 14;46(42):8064-6. doi: 10.1039/c0cc03032e. Epub 2010 Sep 24. Chem Commun (Camb). 2010. PMID: 20865203

10

Enantioselective α-amination of branched aldehydes promoted by simple chiral primary amino acids.

Fu JY, Yang QC, Wang QL, Ming JN, Wang FY, Xu XY, Wang LX. Fu JY, et al. Among authors: xu xy. J Org Chem. 2011 Jun 3;76(11):4661-4. doi: 10.1021/jo102361h. Epub 2011 May 6. J Org Chem. 2011. PMID: 21517112

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