Wang LX - Search Results

1

A cinchona alkaloid catalyzed enantioselective sulfa-Michael/aldol cascade reaction of isoindigos: construction of chiral bispirooxindole tetrahydrothiophenes with vicinal quaternary spirocenters.

Gui YY, Yang J, Qi LW, Wang X, Tian F, Li XN, Peng L, Wang LX. Gui YY, et al. Among authors: wang x, wang lx. Org Biomol Chem. 2015 Jun 14;13(22):6371-9. doi: 10.1039/c5ob00774g. Org Biomol Chem. 2015. PMID: 25974840

2

Highly enantioselective copper-catalyzed conjugate addition of diethylzinc to enones using chiral spiro phosphoramidites as ligands.

Zhou H, Wang WH, Fu Y, Xie JH, Shi WJ, Wang LX, Zhou QL. Zhou H, et al. Among authors: wang lx, wang wh. J Org Chem. 2003 Feb 21;68(4):1582-4. doi: 10.1021/jo026611m. J Org Chem. 2003. PMID: 12585909

3

Copper-catalyzed asymmetric ring opening of oxabicyclic alkenes with Grignard reagents.

Zhang W, Wang LX, Shi WJ, Zhou QL. Zhang W, et al. Among authors: wang lx. J Org Chem. 2005 Apr 29;70(9):3734-6. doi: 10.1021/jo050015l. J Org Chem. 2005. PMID: 15845018

4

Highly enantioselective synthesis of chiral cyclic amino alcohols and conhydrine by ruthenium-catalyzed asymmetric hydrogenation.

Liu S, Xie JH, Li W, Kong WL, Wang LX, Zhou QL. Liu S, et al. Among authors: wang lx. Org Lett. 2009 Nov 5;11(21):4994-7. doi: 10.1021/ol901605a. Org Lett. 2009. PMID: 19788265

5

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: wang lx. Org Biomol Chem. 2010 Oct 21;8(20):4524-6. doi: 10.1039/c0ob00406e. Epub 2010 Aug 23. Org Biomol Chem. 2010. PMID: 20733976

6

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: wang lx. Chem Commun (Camb). 2010 Nov 14;46(42):8064-6. doi: 10.1039/c0cc03032e. Epub 2010 Sep 24. Chem Commun (Camb). 2010. PMID: 20865203

7

A highly organocatalytic stereoselective double Michael reaction: efficient construction of optically enriched spirocyclic oxindoles.

Wang LL, Peng L, Bai JF, Jia LN, Luo XY, Huang QC, Xu XY, Wang LX. Wang LL, et al. Among authors: wang lx. Chem Commun (Camb). 2011 May 21;47(19):5593-5. doi: 10.1039/c1cc11223f. Epub 2011 Apr 1. Chem Commun (Camb). 2011. PMID: 21455513

8

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: wang lx, wang ql, wang fy. J Org Chem. 2011 Jun 3;76(11):4661-4. doi: 10.1021/jo102361h. Epub 2011 May 6. J Org Chem. 2011. PMID: 21517112

9

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: wang lx, wang ll, wang fy. Org Biomol Chem. 2011 Jul 7;9(13):4774-7. doi: 10.1039/c1ob05607g. Epub 2011 May 26. Org Biomol Chem. 2011. PMID: 21614388

10

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: wang lx, wang ll. Org Biomol Chem. 2012 Jan 14;10(2):236-9. doi: 10.1039/c1ob06413d. Epub 2011 Oct 21. Org Biomol Chem. 2012. PMID: 22016069

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