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.
7. Metal-free direct asymmetric aminoxylation of aldehydes catalyzed by a binaphthyl-based chiral amine. Kano T; Mii H; Maruoka K Angew Chem Int Ed Engl; 2010 Sep; 49(37):6638-41. PubMed ID: 20672271 [No Abstract] [Full Text] [Related]
8. Molecular recognition of ketomalonates by asymmetric aldol reaction of aldehydes with secondary-amine organocatalysts. Kano T; Song S; Maruoka K Chem Commun (Camb); 2012 Jul; 48(56):7037-9. PubMed ID: 22684237 [TBL] [Abstract][Full Text] [Related]
9. An organocatalytic Michael-cyclization cascade of 4-oxa-α,β-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral γ-lactols and trisubstituted γ-lactones. Lin JB; Xu SM; Xie JK; Li HY; Xu PF Chem Commun (Camb); 2015 Feb; 51(17):3596-9. PubMed ID: 25633800 [TBL] [Abstract][Full Text] [Related]
10. Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst. Kano T; Ueda M; Maruoka K J Am Chem Soc; 2008 Mar; 130(12):3728-9. PubMed ID: 18321093 [TBL] [Abstract][Full Text] [Related]
11. Asymmetric tandem Michael addition-Wittig reaction to cyclohexenone annulation. Liu YK; Ma C; Jiang K; Liu TY; Chen YC Org Lett; 2009 Jul; 11(13):2848-51. PubMed ID: 19518069 [TBL] [Abstract][Full Text] [Related]
12. A simple primary amine thiourea catalyzed highly enantioselective conjugate addition of alpha,alpha-disubstituted aldehydes to maleimides. Xue F; Liu L; Zhang S; Duan W; Wang W Chemistry; 2010 Jul; 16(27):7979-82. PubMed ID: 20540054 [No Abstract] [Full Text] [Related]
13. A chiral primary amine thiourea catalyst for the highly enantioselective direct conjugate addition of alpha,alpha-disubstituted aldehydes to nitroalkenes. Lalonde MP; Chen Y; Jacobsen EN Angew Chem Int Ed Engl; 2006 Sep; 45(38):6366-70. PubMed ID: 16937417 [No Abstract] [Full Text] [Related]
14. Selectivity control in enantioselective four-component reactions of aryl diazoacetates with alcohols, aldehydes and amines: an efficient approach to synthesizing chiral beta-amino-alpha-hydroxyesters. Xu X; Zhou J; Yang L; Hu W Chem Commun (Camb); 2008 Dec; (48):6564-6. PubMed ID: 19057780 [TBL] [Abstract][Full Text] [Related]
15. Highly enantioselective hetero-Diels-Alder reactions between Rawal's diene and aldehydes catalyzed by chiral dirhodium(II) carboxamidates. Watanabe Y; Washio T; Shimada N; Anada M; Hashimoto S Chem Commun (Camb); 2009 Dec; (47):7294-6. PubMed ID: 20024206 [TBL] [Abstract][Full Text] [Related]
16. Highly enantioselective michael addition of cyclic 1,3-dicarbonyl compounds to alpha,beta-unsaturated ketones. Xie JW; Yue L; Chen W; Du W; Zhu J; Deng JG; Chen YC Org Lett; 2007 Feb; 9(3):413-5. PubMed ID: 17249775 [TBL] [Abstract][Full Text] [Related]
17. Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis. Han B; Xiao YC; He ZQ; Chen YC Org Lett; 2009 Oct; 11(20):4660-3. PubMed ID: 19754072 [TBL] [Abstract][Full Text] [Related]
18. Highly enantio- and diastereoselective organocatalytic cascade aza-Michael-Michael reactions: a direct method for the synthesis of trisubstituted chiral pyrrolidines. Li H; Zu L; Xie H; Wang J; Wang W Chem Commun (Camb); 2008 Nov; (43):5636-8. PubMed ID: 18997977 [TBL] [Abstract][Full Text] [Related]
19. Catalytic enantioselective construction of all-carbon quaternary stereocenters by an organocatalytic Diels-Alder reaction of alpha-substituted alpha,beta-unsaturated aldehydes. Kano T; Tanaka Y; Osawa K; Yurino T; Maruoka K Chem Commun (Camb); 2009 Apr; (15):1956-8. PubMed ID: 19333455 [TBL] [Abstract][Full Text] [Related]
20. Copper-catalyzed enantioselective three-component synthesis of optically active propargylamines from aldehydes, amines, and aliphatic alkynes. Nakamura S; Ohara M; Nakamura Y; Shibata N; Toru T Chemistry; 2010 Feb; 16(8):2360-2. PubMed ID: 20108286 [No Abstract] [Full Text] [Related] [Next] [New Search]