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5. One-pot organocatalytic enantioselective domino double-Michael reaction and Pictet-Spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers. Hong BC; Liao WK; Dange NS; Liao JH Org Lett; 2013 Feb; 15(3):468-71. PubMed ID: 23311855 [TBL] [Abstract][Full Text] [Related]
6. A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction. Tan B; Chua PJ; Zeng X; Lu M; Zhong G Org Lett; 2008 Aug; 10(16):3489-92. PubMed ID: 18630924 [TBL] [Abstract][Full Text] [Related]
7. Domino alkylation/oxa-Michael of 1,3-cyclohexanediones: steering the C/O-chemoselectivity to reach tetrahydrobenzofuranones. Devi RB; Henrot M; De Paolis M; Maddaluno J Org Biomol Chem; 2011 Oct; 9(19):6509-12. PubMed ID: 21826296 [TBL] [Abstract][Full Text] [Related]
8. Stereoselective synthesis of highly functionalized nitrocyclopropanes through the organocatalyic Michael-addition-initiated cyclization of bromonitromethane and β,γ-unsaturated α-ketoesters. Yu H; Wang Q; Wang Y; Song H; Zhou Z; Tang C Chem Asian J; 2013 Nov; 8(11):2859-63. PubMed ID: 23934622 [TBL] [Abstract][Full Text] [Related]
9. Control of four stereocenters in an organocatalytic domino double Michael reaction: efficient synthesis of multisubstituted cyclopentanes. Tan B; Shi Z; Chua PJ; Zhong G Org Lett; 2008 Aug; 10(16):3425-8. PubMed ID: 18616339 [TBL] [Abstract][Full Text] [Related]
10. Unique Michael addition-initiated domino reaction for the stereoselective synthesis of functionalized macrolactones from alpha-nitroketones in water. Giorgi G; Miranda S; López-Alvarado P; Avendaño C; Rodriguez J; Menéndez JC Org Lett; 2005 May; 7(11):2197-200. PubMed ID: 15901168 [TBL] [Abstract][Full Text] [Related]
11. The MARDi cascade: a Michael-initiated domino-multicomponent approach for the stereoselective synthesis of seven-membered rings. Coquerel Y; Filippini MH; Bensa D; Rodriguez J Chemistry; 2008; 14(10):3078-92. PubMed ID: 18257007 [TBL] [Abstract][Full Text] [Related]
12. Stereoselective desymmetrisation of prochiral alpha,alpha-dicyanoalkenes via domino Michael-Michael addition reactions. Kang TR; Xie JW; Du W; Feng X; Chen YC Org Biomol Chem; 2008 Aug; 6(15):2673-5. PubMed ID: 18633522 [TBL] [Abstract][Full Text] [Related]
13. Organocatalytic Oxa-Michael/Michael/Michael/Aldol Condensation Quadruple Domino Sequence: Asymmetric Synthesis of Tricyclic Chromanes. Kumar M; Chauhan P; Bailey SJ; Jafari E; von Essen C; Rissanen K; Enders D Org Lett; 2018 Feb; 20(4):1232-1235. PubMed ID: 29406738 [TBL] [Abstract][Full Text] [Related]
14. Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet-Spengler reaction. Verma AK; Chennaiah A; Dubbu S; Vankar YD Org Biomol Chem; 2018 Sep; 16(37):8258-8262. PubMed ID: 30204196 [TBL] [Abstract][Full Text] [Related]
15. Stereoselective synthesis of substituted tetrahydropyrans via domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization. Fuwa H; Noto K; Sasaki M Org Lett; 2010 Apr; 12(7):1636-9. PubMed ID: 20222688 [TBL] [Abstract][Full Text] [Related]
16. New multicomponent cyclization: domino synthesis of pentasubstituted pyridines under solvent-free conditions. Jiang B; Wang X; Shi F; Tu SJ; Li G Org Biomol Chem; 2011 Jun; 9(11):4025-8. PubMed ID: 21523293 [TBL] [Abstract][Full Text] [Related]
17. Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons. Jiang B; Wang X; Xu HW; Tu MS; Tu SJ; Li G Org Lett; 2013 Apr; 15(7):1540-3. PubMed ID: 23506186 [TBL] [Abstract][Full Text] [Related]
18. Diastereoselective synthesis of delta-aminoacids through domino Ireland-Claisen rearrangement and Michael addition. Garrido NM; García M; Díez D; Sánchez MR; Sanz F; Urones JG Org Lett; 2008 May; 10(9):1687-90. PubMed ID: 18399652 [TBL] [Abstract][Full Text] [Related]