Ryo Takita
Affiliations: | 2007- | Kyoto University, Kyōto-shi, Kyōto-fu, Japan |
Area:
Synthetic Organic ChemistryWebsite:
http://rdb.kuicr.kyoto-u.ac.jp/researchers/view/takita+ryo/enGoogle:
"Ryo Takita"Mean distance: 7.18 | S | N | B | C | P |
Parents
Sign in to add mentorMasanobu Uchiyama | grad student | The University of Tokyo (Japan) | |
Masakatsu Shibasaki | grad student | 2006 | Tokyo University |
Timothy M. Swager | post-doc | 2006-2007 | MIT |
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Publications
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Yamashita K, Hirokawa R, Ichikawa M, et al. (2022) Mechanistic Details of Asymmetric Bromocyclization with BINAP Monoxide: Identification of Chiral Proton-Bridged Bisphosphine Oxide Complex and Its Application to Parallel Kinetic Resolution. Journal of the American Chemical Society. 144: 3913-3924 |
Nakamura T, Yoshida E, Hara T, et al. (2020) Zn(ii)2,9-dimethyl-1,10-phenanthroline stimulates cultured bovine aortic endothelial cell proliferation. Rsc Advances. 10: 42327-42337 |
Watanabe K, Takagi M, Watanabe A, et al. (2020) Cu(I)/sucrose-catalyzed hydroxylation of arenes in water: the dual role of sucrose. Organic & Biomolecular Chemistry |
Wang B, Li Y, Pang JH, et al. (2020) Hydromagnesiation of 1,3-enynes by magnesium hydride for synthesis of tri- and tetra-substituted allenes. Angewandte Chemie (International Ed. in English) |
Wang B, Ong DY, Li Y, et al. (2020) Stereo-controlled anti-hydromagnesiation of aryl alkynes by magnesium hydrides Chemical Science. 11: 5267-5272 |
Oi M, Takita R, Kanazawa J, et al. (2019) Organocopper cross-coupling reaction for C-C bond formation on highly sterically hindered structures. Chemical Science. 10: 6107-6112 |
Pang JH, Ong DY, Watanabe K, et al. (2019) Leaving Group Ability in Nucleophilic Aromatic Amination by Sodium Hydride–Lithium Iodide Composite Synthesis. 52: 393-398 |
Takagi M, Watanabe A, Murata S, et al. (2018) Copper-catalyzed arene amination in pure aqueous ammonia. Organic & Biomolecular Chemistry |
Akimoto G, Otsuka M, Takita R, et al. (2018) Deprotonative Metalation of Methoxy-Substituted Arenes Using Lithium 2,2,6,6-Tetramethylpiperidide: Experimental and Computational Study. The Journal of Organic Chemistry. 83: 13498-13506 |
Kato N, Nogawa T, Takita R, et al. (2018) Control of the Stereochemical Course of [4+2] Cycloaddition during trans-Decalin Formation by Fsa2-Family Enzymes. Angewandte Chemie (International Ed. in English) |