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.
4. Highly enantioselective synthesis of chiral 3-substituted indolines by catalytic asymmetric hydrogenation of indoles. Kuwano R; Kaneda K; Ito T; Sato K; Kurokawa T; Ito Y Org Lett; 2004 Jun; 6(13):2213-5. PubMed ID: 15200323 [TBL] [Abstract][Full Text] [Related]
5. Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes. Makida Y; Saita M; Kuramoto T; Ishizuka K; Kuwano R Angew Chem Int Ed Engl; 2016 Sep; 55(39):11859-62. PubMed ID: 27561154 [TBL] [Abstract][Full Text] [Related]
6. Catalytic asymmetric hydrogenation of quinoline carbocycles: unusual chemoselectivity in the hydrogenation of quinolines. Kuwano R; Ikeda R; Hirasada K Chem Commun (Camb); 2015 May; 51(35):7558-61. PubMed ID: 25847758 [TBL] [Abstract][Full Text] [Related]
7. Ruthenium-Catalyzed Chemo- and Enantioselective Hydrogenation of Isoquinoline Carbocycles. Jin Y; Makida Y; Uchida T; Kuwano R J Org Chem; 2018 Apr; 83(7):3829-3839. PubMed ID: 29547282 [TBL] [Abstract][Full Text] [Related]
8. Highly efficient and enantioselective hydrogenation of quinolines and pyridines with Ir-Difluorphos catalyst. Tang W; Sun Y; Lijin Xu ; Wang T; Qinghua Fan ; Lam KH; Chan AS Org Biomol Chem; 2010 Aug; 8(15):3464-71. PubMed ID: 20532262 [TBL] [Abstract][Full Text] [Related]
9. Highly enantioselective hydrogenation of quinolines using phosphine-free chiral cationic ruthenium catalysts: scope, mechanism, and origin of enantioselectivity. Wang T; Zhuo LG; Li Z; Chen F; Ding Z; He Y; Fan QH; Xiang J; Yu ZX; Chan AS J Am Chem Soc; 2011 Jun; 133(25):9878-91. PubMed ID: 21574550 [TBL] [Abstract][Full Text] [Related]
10. Chiral eta(6)-arene/N-tosylethylenediamine-ruthenium(II) complexes: solution behavior and catalytic activity for asymmetric hydrogenation. Sandoval CA; Bie F; Matsuoka A; Yamaguchi Y; Naka H; Li Y; Kato K; Utsumi N; Tsutsumi K; Ohkuma T; Murata K; Noyori R Chem Asian J; 2010 Apr; 5(4):806-16. PubMed ID: 20235268 [TBL] [Abstract][Full Text] [Related]
11. Mechanism of asymmetric hydrogenation of acetophenone catalyzed by chiral eta(6)-arene-N-tosylethylenediamine-ruthenium(II) complexes. Sandoval CA; Ohkuma T; Utsumi N; Tsutsumi K; Murata K; Noyori R Chem Asian J; 2006 Jul; 1(1-2):102-10. PubMed ID: 17441044 [TBL] [Abstract][Full Text] [Related]
12. The hydrogenation/transfer hydrogenation network: asymmetric hydrogenation of ketones with chiral eta6-arene/N-Tosylethylenediamine-ruthenium(II) catalysts. Ohkuma T; Utsumi N; Tsutsumi K; Murata K; Sandoval C; Noyori R J Am Chem Soc; 2006 Jul; 128(27):8724-5. PubMed ID: 16819854 [TBL] [Abstract][Full Text] [Related]
13. Synthesis and application of chiral N-heterocyclic carbene-oxazoline ligands: iridium-catalyzed enantioselective hydrogenation. Nanchen S; Pfaltz A Chemistry; 2006 Jun; 12(17):4550-8. PubMed ID: 16557626 [TBL] [Abstract][Full Text] [Related]
14. New chiral ruthenium(II) catalysts containing 2,6-bis(4'-(R)-phenyloxazolin-2'-yl)pyridine (Ph-pybox) ligands for highly enantioselective transfer hydrogenation of ketones. Cuervo D; Gamasa MP; Gimeno J Chemistry; 2004 Jan; 10(2):425-32. PubMed ID: 14735511 [TBL] [Abstract][Full Text] [Related]
15. CeCl3.7H2O: an effective additive in Ru-catalyzed enantioselective hydrogenation of aromatic alpha-ketoesters. Meng Q; Sun Y; Ratovelomanana-Vidal V; Genêt JP; Zhang Z J Org Chem; 2008 May; 73(10):3842-7. PubMed ID: 18429633 [TBL] [Abstract][Full Text] [Related]
16. Asymmetric hydrogenation of N-sulfonylated-alpha-dehydroamino acids: toward the synthesis of an anthrax lethal factor inhibitor. Shultz CS; Dreher SD; Ikemoto N; Williams JM; Grabowski EJ; Krska SW; Sun Y; Dormer PG; Dimichele L Org Lett; 2005 Aug; 7(16):3405-8. PubMed ID: 16048303 [TBL] [Abstract][Full Text] [Related]
17. Asymmetric hydrogenation of aromatic ketones catalyzed by the TolBINAP/DMAPEN-ruthenium(II) complex: a significant effect of N-substituents of chiral 1,2-diamine ligands on enantioselectivity. Ooka H; Arai N; Azuma K; Kurono N; Ohkuma T J Org Chem; 2008 Nov; 73(22):9084-93. PubMed ID: 18925787 [TBL] [Abstract][Full Text] [Related]
18. Employing the structural diversity of nature: development of modular dipeptide-analogue ligands for ruthenium-catalyzed enantioselective transfer hydrogenation of ketones. Pastor IM; Västilä P; Adolfsson H Chemistry; 2003 Sep; 9(17):4031-45. PubMed ID: 12953189 [TBL] [Abstract][Full Text] [Related]
19. Development of 4,4'-substituted-XylBINAP ligands for highly enantioselective hydrogenation of ketones. Ngo HL; Lin W J Org Chem; 2005 Feb; 70(4):1177-87. PubMed ID: 15704949 [TBL] [Abstract][Full Text] [Related]
20. A succession of isomers of ruthenium dihydride complexes. Which one is the ketone hydrogenation catalyst? Abbel R; Abdur-Rashid K; Faatz M; Hadzovic A; Lough AJ; Morris RH J Am Chem Soc; 2005 Feb; 127(6):1870-82. PubMed ID: 15701022 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]