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Volumn 48, Issue 7, 2009, Pages 1324-1327

Hydrogenation of N-acylcarbamates and N-acylsulfonamides catalyzed by a bifunctional [Cp*Ru(PN)] complex

Author keywords

Alcohols; Enantioselectivity; Hydrogenation ligand effects; Ruthenium

Indexed keywords

AMINES; ELECTRON TRANSITIONS; ENANTIOSELECTIVITY; HYDROCARBONS; KETONES; LIGANDS; RUTHENIUM;

EID: 60149095135     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200805307     Document Type: Article
Times cited : (72)

References (46)
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    • For the mechanistic aspect of Noyori's hydrogenation, see: a) K. Abdur-Rashid, M. Faatz, A. J. Lough, R. H. Morris, J. Am. Chem. Soc. 2001, 123, 7473-7474;
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    • Abdur-Rashid, K.1    Faatz, M.2    Lough, A.J.3    Morris, R.H.4
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    • On the Ru/NH bifunctionality: a R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102;
    • On the Ru/NH bifunctionality: a) R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102;
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    • For 5c:C13H17NO3S, orthorhombic, P212121, a, 8,289(3, b, 10.605(4, c, 15.237(6) Å, V, 1339.3(9) Å3, Z, 4,pcalcd, 1.326 gcm -3, F000, 568.00, μ, 2.415 cirr-1, transmission factors: 0.812-0.930, reflections measured 10632, independent reflections 3045, R1, 0.0339 [I > 2s(I, wR2, 0.0992 (all data, residual electron density 0.35/-0.39 e Å-3. Data were collected at 193 K using a Rigaku Saturn CCD area detector with graphite-monochromated Mo Ka radiation (λ, 0.7107 Å) to a maximum 2θ value of 55°. Intensity data were corrected for Lorentz-polarization effects and for absorption. Structure solution and refinements were performed with the CrystalStructure program package.[13] The structures were refined against F2 with an
    • 2 with anisotropic temperature factors for all non-hydrogen atoms. All hydrogen atoms were added geometrically and refined by using a riding model. CCDC705015 (2e), 705016 (4c), and 705017 (5c) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif;
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    • [12] Preliminary results were disclosed in our recent review article: M. Ito, T. Ikariya, J. Synth. Org. Chem. Jpn. 2008, 66, 1042-1048.
    • [12] Preliminary results were disclosed in our recent review article: M. Ito, T. Ikariya, J. Synth. Org. Chem. Jpn. 2008, 66, 1042-1048.
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    • Very recently, the groups of Milstein and Firmenich have independently developed excellent catalyst systems for the hydrogenation of esters: a J. Zhang, G. Leitus, Y. Ben-David, D. Milstein, Angew. Chem. 2006, 118, 1131-1133;
    • Very recently, the groups of Milstein and Firmenich have independently developed excellent catalyst systems for the hydrogenation of esters: a) J. Zhang, G. Leitus, Y. Ben-David, D. Milstein, Angew. Chem. 2006, 118, 1131-1133;
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.