Account of Nishi Lab

総合論文 [Accounts]

Y. Naganawa, H. Nishiyama
Renovation of Optically Active Phenanthroline as Powerful Chiral Ligands for Versatile Asymmetric Metal Catalysis
Chem. Rec. in press.

西山久雄
使ってもらえる光学活性窒素配位子の開発
有機合成化学協会誌、2015年、第73巻、925−931頁(ラウンジ)

Hisao Nishiyama
Usable optically active nitrogen-based tridentate ligands for asymmetric catalysis
J. Synth. Org. Chem. Jpn., 2015, 73, 925-931. (Lounge)

Nishiyama, H.
Bis(acetato)aqua[2,6-bis[(4S)-4,5-dihydro-4-(1-methylethyl)-2-oxazolyl]-phenyl]rhodium
e-EROS Encyclopedia of Reagents for Organic Synthesis, Wiley Online Library (2014)
DOI: 10.1002/047084289X.rn01765

Ito, J.; Nishiyama, H.
Ruthenium, [2,6-bis[4,5-dihydro-4-(1-methylethyl)-2-oxazolyl-κN3]pyridine-κN]dichloro(η2-ethene)-, stereoisomer
e-EROS Encyclopedia of Reagents for Organic Synthesis, Wiley Online Library (2014)
DOI: 10.1002/047084289X.rn01747

Ito, J.; Nishiyama, H.
Recent topics of transfer hydrogenation
Tetrahedron Lett. 2014, 55, 3133-3146.
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Ito, J.; Nishiyama, H.
Asymmetric Catalysis Mediated by Optically Active Bis(oxazolinyl)phenyl Metal Complexes
J. Synth. Org. Chem. Jpn. 2013, 71, 791-803.

Ito, J.; Nishiyama, H.
Synthetic Utility of Chiral Bis(oxazolinyl)phenyl Transition-Metal Complexes
Synlett 2012, 23, 509-523
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Nishiyama,H.; Ito, J.
Bis(oxazolinyl)phenyl Transition-metal Complexes: Asymmetric Catalysis and Some Reactions of the Metals
Chem. Commun. 2010, 46, 203-212 [Feature Article]
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Nishiyama, H.; Ito, J.; Shiomi, T.; Hashimoto, T.; Miyakawa, T.; Kitase, M.
Chiral phenyl-bis(oxazoline) as an efficient auxiliary for asymmetric catalysis
Pure Appl. Chem. 2008, 80, 743-749.

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Nishiyama, H.
Synthesis and use of bisoxazolinyl-phenyl pincers
Chem. Soc. Rev. 2007, 36, 1133-1141.

Nishiyama, H.; Ito, J.
Bis(oxazolinyl)phenyl Transition Metal Complexes: Synthesis, Asymmetric Catalysis, and Coordination Chemistry
Chem. Rec. 2007, 7, 159-166.

Motoyama, Y.; Nishiyama, H.
Chiral transition metal Lewis acids bearing bis(oxazolinyl)phenyl (Phebox) as a pincer ligand: Synthesis and application for the asymmetric reactions
J. Synth. Org. Chem. Jpn.
2003, 61, 343-351.