Similar articles for PMID: 20865203

Year	Number of Results
1997	1
1999	2
2000	1
2001	1
2002	3
2003	2
2004	1
2005	5
2006	7
2007	12
2008	10
2009	10
2010	35
2011	18
2012	19
2013	21
2014	21
2015	21
2016	16
2017	15
2018	21
2019	22
2020	14
2021	15
2022	13
2023	4
2024	0

1

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

2

Synthesis of six-membered spirocyclic oxindoles with five consecutive stereocenters in an asymmetric organocatalytic one-pot Michael/Michael/aldol addition sequence.

Zhou B, Yang Y, Shi J, Luo Z, Li Y. Zhou B, et al. J Org Chem. 2013 Apr 5;78(7):2897-907. doi: 10.1021/jo302655u. Epub 2013 Mar 8. J Org Chem. 2013. PMID: 23469872

3

Organocatalytic tandem reaction to construct six-membered spirocyclic oxindoles with multiple chiral centres through a formal [2+2+2] annulation.

Jiang K, Jia ZJ, Chen S, Wu L, Chen YC. Jiang K, et al. Chemistry. 2010 Mar 1;16(9):2852-6. doi: 10.1002/chem.200903009. Chemistry. 2010. PMID: 20112315

4

Organocatalytic Asymmetric Michael/Friedel-Crafts Cascade Reaction of 3-Pyrrolyl-oxindoles and α,β-Unsaturated Aldehydes for the Construction of Chiral Spiro[5,6-dihydropyrido[1,2-a]pyrrole-3,3'-oxindoles].

You Y, Cui BD, Zhou MQ, Zuo J, Zhao JQ, Xu XY, Zhang XM, Yuan WC. You Y, et al. J Org Chem. 2015 Jun 5;80(11):5951-7. doi: 10.1021/acs.joc.5b00597. Epub 2015 May 26. J Org Chem. 2015. PMID: 25984596

5

Organocatalytic asymmetric synthesis of polyfunctionalized 3-(cyclohexenylmethyl)-indoles via a quadruple domino Friedel-Crafts-type/Michael/Michael/aldol condensation reaction.

Enders D, Wang C, Mukanova M, Greb A. Enders D, et al. Chem Commun (Camb). 2010 Apr 14;46(14):2447-9. doi: 10.1039/c002839h. Epub 2010 Mar 8. Chem Commun (Camb). 2010. PMID: 20309466

6

Organocatalytic direct asymmetric aldol reactions of 3-isothiocyanato oxindoles to ketones: stereocontrolled synthesis of spirooxindoles bearing highly congested contiguous tetrasubstituted stereocenters.

Chen WB, Wu ZJ, Hu J, Cun LF, Zhang XM, Yuan WC. Chen WB, et al. Org Lett. 2011 May 6;13(9):2472-5. doi: 10.1021/ol200724q. Epub 2011 Apr 7. Org Lett. 2011. PMID: 21473612

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. Chem Commun (Camb). 2014 Dec 4;50(93):14601-4. doi: 10.1039/c4cc05207b. Chem Commun (Camb). 2014. PMID: 25307364

8

An organocatalytic Michael-aldol cascade: formal [3+2] annulation to construct enantioenriched spirocyclic oxindole derivatives.

Duan SW, Li Y, Liu YY, Zou YQ, Shi DQ, Xiao WJ. Duan SW, et al. Chem Commun (Camb). 2012 May 25;48(42):5160-2. doi: 10.1039/c2cc30931a. Epub 2012 Mar 21. Chem Commun (Camb). 2012. PMID: 22434093

9

Organocatalytic asymmetric tandem Michael-Henry reactions: a highly stereoselective synthesis of multifunctionalized cyclohexanes with two quaternary stereocenters.

Tan B, Chua PJ, Li Y, Zhong G. Tan B, et al. Org Lett. 2008 Jun 19;10(12):2437-40. doi: 10.1021/ol8007183. Epub 2008 May 20. Org Lett. 2008. PMID: 18489178

10

An asymmetric approach toward chiral multicyclic spirooxindoles from isothiocyanato oxindoles and unsaturated pyrazolones by a chiral tertiary amine thiourea catalyst.

Chen Q, Liang J, Wang S, Wang D, Wang R. Chen Q, et al. Chem Commun (Camb). 2013 Feb 25;49(16):1657-9. doi: 10.1039/c3cc38386e. Chem Commun (Camb). 2013. PMID: 23334197

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