These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
265 related articles for article (PubMed ID: 25317757)
1. A Mannich/cyclization cascade process for the asymmetric synthesis of spirocyclic thioimidazolidineoxindoles. Cai H; Zhou Y; Zhang D; Xu J; Liu H Chem Commun (Camb); 2014 Dec; 50(94):14771-4. PubMed ID: 25317757 [TBL] [Abstract][Full Text] [Related]
2. 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 J Org Chem; 2015 Jun; 80(11):5951-7. PubMed ID: 25984596 [TBL] [Abstract][Full Text] [Related]
3. 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 Chem Commun (Camb); 2013 Feb; 49(16):1657-9. PubMed ID: 23334197 [TBL] [Abstract][Full Text] [Related]
4. Asymmetric one-pot sequential Mannich/hydroamination reaction by organo- and gold catalysts: synthesis of spiro[pyrrolidin-3,2'-oxindole] derivatives. Chen X; Chen H; Ji X; Jiang H; Yao ZJ; Liu H Org Lett; 2013 Apr; 15(8):1846-9. PubMed ID: 23560725 [TBL] [Abstract][Full Text] [Related]
5. 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 Chemistry; 2010 Mar; 16(9):2852-6. PubMed ID: 20112315 [TBL] [Abstract][Full Text] [Related]
6. Asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles and 3-nitroindoles with amino-thiocarbamate catalysts: enantioselective synthesis of polycyclic spirooxindoles. Zhao JQ; Zhou MQ; Wu ZJ; Wang ZH; Yue DF; Xu XY; Zhang XM; Yuan WC Org Lett; 2015 May; 17(9):2238-41. PubMed ID: 25875402 [TBL] [Abstract][Full Text] [Related]
7. Direct enantioselective vinylogous aldol-cyclization cascade reaction of allyl pyrazoleamides with isatins: asymmetric construction of spirocyclic oxindole-dihydropyranones. Li TZ; Jiang Y; Guan YQ; Sha F; Wu XY Chem Commun (Camb); 2014 Sep; 50(74):10790-2. PubMed ID: 25019965 [TBL] [Abstract][Full Text] [Related]
8. Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates. Kayal S; Mukherjee S Org Lett; 2015 Nov; 17(21):5508-11. PubMed ID: 26512732 [TBL] [Abstract][Full Text] [Related]
9. Catalytic asymmetric construction of spiro[pyrrolidine-2,3'-oxindole] scaffolds through chiral phosphoric acid-catalyzed 1,3-dipolar cycloaddition involving 3-amino oxindoles. Zhu G; Wang B; Bao X; Zhang H; Wei Q; Qu J Chem Commun (Camb); 2015 Nov; 51(85):15510-3. PubMed ID: 26345264 [TBL] [Abstract][Full Text] [Related]
10. 3-isothiocyanato oxindoles serving as powerful and versatile precursors to structurally diverse dispirocyclic thiopyrrolidineoxindoles through a cascade Michael/cyclization process with amino-thiocarbamate catalysts. Han WY; Li SW; Wu ZJ; Zhang XM; Yuan WC Chemistry; 2013 Apr; 19(18):5551-6. PubMed ID: 23495169 [TBL] [Abstract][Full Text] [Related]
12. N-Heterocyclic carbene-catalyzed [4 + 2] cyclization of α,β-unsaturated carboxylic acids bearing γ-H with isatins: an enantioselective synthesis of spirocyclic oxindole-dihydropyranones. Zhu L; Yu C; Li T; Wang Y; Lu Y; Wang W; Yao C Org Biomol Chem; 2016 Jan; 14(4):1485-91. PubMed ID: 26690686 [TBL] [Abstract][Full Text] [Related]
13. 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 Chem Commun (Camb); 2012 May; 48(42):5160-2. PubMed ID: 22434093 [TBL] [Abstract][Full Text] [Related]
14. Tandem Michael addition-ring transformation reactions of 3-hydroxyoxindoles/3-aminooxindoles with olefinic azlactones: direct access to structurally diverse spirocyclic oxindoles. Cui BD; Zuo J; Zhao JQ; Zhou MQ; Wu ZJ; Zhang XM; Yuan WC J Org Chem; 2014 Jun; 79(11):5305-14. PubMed ID: 24785087 [TBL] [Abstract][Full Text] [Related]
15. Squaramide-Catalyzed Synthesis of Enantioenriched Spirocyclic Oxindoles via Ketimine Intermediates with Multiple Active Sites. Sun QS; Zhu H; Chen YJ; Yang XD; Sun XW; Lin GQ Angew Chem Int Ed Engl; 2015 Nov; 54(45):13253-7. PubMed ID: 26337819 [TBL] [Abstract][Full Text] [Related]
16. Asymmetric pericyclic cascade approach to spirocyclic oxindoles. Richmond E; Duguet N; Slawin AM; Lébl T; Smith AD Org Lett; 2012 Jun; 14(11):2762-5. PubMed ID: 22583112 [TBL] [Abstract][Full Text] [Related]
17. Highly efficient enantioselective construction of bispirooxindoles containing three stereocenters through an organocatalytic cascade Michael-cyclization reaction. Wu H; Zhang LL; Tian ZQ; Huang YD; Wang YM Chemistry; 2013 Jan; 19(5):1747-53. PubMed ID: 23255327 [TBL] [Abstract][Full Text] [Related]
18. An organocatalytic Mannich/denitration reaction for the asymmetric synthesis of 3-ethylacetate-substitued 3-amino-2-oxindoles: formal synthesis of AG-041R. Zhao K; Shu T; Jia J; Raabe G; Enders D Chemistry; 2015 Mar; 21(10):3933-6. PubMed ID: 25630891 [TBL] [Abstract][Full Text] [Related]
19. Highly efficient and stereocontrolled construction of 3,3'-pyrrolidonyl spirooxindoles via organocatalytic domino Michael/cyclization reaction. Liu XL; Han WY; Zhang XM; Yuan WC Org Lett; 2013 Mar; 15(6):1246-9. PubMed ID: 23452297 [TBL] [Abstract][Full Text] [Related]
20. Multicomponent reaction to construct spirocyclic oxindoles with a Michael (triple Michael)/cyclization cascade sequence as the key step. Li J; Wang N; Li C; Jia X Chemistry; 2012 Jul; 18(31):9645-50. PubMed ID: 22815218 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]