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Volumn 14, Issue 7, 2011, Pages 1161-1164

Ru(II) xantphos complex as an efficient catalyst in transfer hydrogenation of carbonyl compounds

Author keywords

C H... interaction; Hydrogen bonding; Ruthenium complex; Transfer hydrogenation; X ray crystallography; Xantphos

Indexed keywords


EID: 79957610939     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2011.04.013     Document Type: Article
Times cited : (15)

References (27)
  • 1
    • 44649156582 scopus 로고    scopus 로고
    • Trans-chelating diphosphines, the elusive ligands!
    • Z. Freixa, P.W.N.M. van Leeuwen, Trans-chelating diphosphines, the elusive ligands! Coord. Chem. Rev. 252 (2008) 1755-1786.
    • (2008) Coord. Chem. Rev. , vol.252 , pp. 1755-1786
    • Freixa, Z.1    Van Leeuwen, P.W.N.M.2
  • 2
    • 0035200787 scopus 로고    scopus 로고
    • Wide bite angle diphosphines: Xantphos ligands in transition metal complexes and catalysis
    • DOI 10.1021/ar000060+
    • P.C.J. Kamer, P.W.N.M. van Leeuwen, J.N.H. Reek, Wide bite angle diphosphines: xantphos ligands in transition metal complexes and catalysis, Acc. Chem. Res. 34 (2001) 895-904. (Pubitemid 33104943)
    • (2001) Accounts of Chemical Research , vol.34 , Issue.11 , pp. 895-904
    • Kamer, P.C.J.1    Van Leeuwen, P.W.N.M.2    Reek, J.N.H.3
  • 3
    • 0036322211 scopus 로고    scopus 로고
    • Excited state properties of transition metal phosphine complexes
    • A. Vogler, H. Kunkely, Excited state properties of transition metal phosphine complexes, Coord. Chem. Rev. 230 (2002) 243-251.
    • (2002) Coord. Chem. Rev. , vol.230 , pp. 243-251
    • Vogler, A.1    Kunkely, H.2
  • 4
    • 0032578172 scopus 로고    scopus 로고
    • Sterically hindered chelating alkyl phosphines provide large rate accelerations in palladium-catalyzed amination of aryl iodides, bromides, and chlorides, and the first amination of aryl tosylates
    • B.C. Hamann, J.F. Hartwig, Sterically hindered chelating alkyl phosphines provide large rate accelerations in palladium-catalyzed amination of aryl iodides, bromides, and chlorides, and the first amination of aryl tosylates, J. Am. Chem. Soc. 120 (1998) 7369-7370.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 7369-7370
    • Hamann, B.C.1    Hartwig, J.F.2
  • 8
    • 3042680897 scopus 로고    scopus 로고
    • Bite angle effects in diphosphine metal catalysts: Steric or electronic?
    • Z. Freixa, P.W.N.M. van Leeuwen, Bite angle effects in diphosphine metal catalysts: steric or electronic? Dalton Trans. (2003) 1890-1901.
    • (2003) Dalton Trans. , pp. 1890-1901
    • Freixa, Z.1    Van Leeuwen, P.W.N.M.2
  • 10
    • 67649378424 scopus 로고    scopus 로고
    • Synthesis of coumarin derivatives by palladium complex catalyzed intramolecular Heck reaction: Preparation of a 1,2-cyclobutadiene-substituted CpCoCb diphosphine chelated palladium complex
    • C.P. Chang, S.V. Pradiuldi, F.E. Hong, Synthesis of coumarin derivatives by palladium complex catalyzed intramolecular Heck reaction: preparation of a 1,2-cyclobutadiene-substituted CpCoCb diphosphine chelated palladium complex, Inorg. Chem. Commun. 12 (2009) 596-598.
    • (2009) Inorg. Chem. Commun. , vol.12 , pp. 596-598
    • Chang, C.P.1    Pradiuldi, S.V.2    Hong, F.E.3
  • 11
    • 17544380569 scopus 로고    scopus 로고
    • Substituent effects in the ruthenium catalyzed hydrosilylation of para-substituted phenylacetylenes
    • DOI 10.1016/j.inoche.2005.02.003, PII S138770030500047X
    • S.I.M. Paris, F.R. Lemke, Substituent effects in the ruthenium catalyzed hydrosilylation of para-substituted phenylacetylenes, Inorg. Chem. Commun. 8 (2005) 425-428. (Pubitemid 40554206)
    • (2005) Inorganic Chemistry Communications , vol.8 , Issue.5 , pp. 425-428
    • Paris, S.I.M.1    Lemke, F.R.2
  • 13
    • 0035385137 scopus 로고    scopus 로고
    • Non-metathesis ruthenium-catalyzed C - C bond formation
    • B.M. Trost, F.D. Toste, A.B. Pinkerton, Non-metathesis ruthenium-catalyzed C - C bond formation, Chem. Rev. 101 (2001) 2067-2096.
    • (2001) Chem. Rev. , vol.101 , pp. 2067-2096
    • Trost, B.M.1    Toste, F.D.2    Pinkerton, A.B.3
  • 14
    • 42149095410 scopus 로고    scopus 로고
    • Mechanisms of water oxidation catalyzed by ruthenium diimine complexes
    • J.K. Hurst, J.L. Cape, A.E. Clark, S. Das, C. Qin, Mechanisms of water oxidation catalyzed by ruthenium diimine complexes, Inorg. Chem. 47 (2008) 1753-1764.
    • (2008) Inorg. Chem. , vol.47 , pp. 1753-1764
    • Hurst, J.K.1    Cape, J.L.2    Clark, A.E.3    Das, S.4    Qin, C.5
  • 15
    • 26944475698 scopus 로고
    • Selective oxygenation of aliphatic ethers catalyzed by ruthenium(II) complexes
    • M. Bressan, A. Morvillo, G. Romanello, Selective oxygenation of aliphatic ethers catalyzed by ruthenium(II) complexes, Inorg. Chem. 29 (1990) 2976-2979.
    • (1990) Inorg. Chem. , vol.29 , pp. 2976-2979
    • Bressan, M.1    Morvillo, A.2    Romanello, G.3
  • 16
    • 61849170693 scopus 로고    scopus 로고
    • Ruthenium-catalyzed cyclodimerization of allenynes
    • N. Saito, Y. Tanaka, Y. Sato, Ruthenium-catalyzed cyclodimerization of allenynes, Organometallics 28 (2009) 669-671.
    • (2009) Organometallics , vol.28 , pp. 669-671
    • Saito, N.1    Tanaka, Y.2    Sato, Y.3
  • 18
    • 0001034905 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation of benzaldehydes
    • I. Yamada, R. Noyori, Asymmetric transfer hydrogenation of benzaldehydes, Org. Lett. 2 (2000) 3425-3427.
    • (2000) Org. Lett. , vol.2 , pp. 3425-3427
    • Yamada, I.1    Noyori, R.2
  • 20
    • 77956406920 scopus 로고    scopus 로고
    • Pyridine-2,6-bis(thioether) (SNS) complexes of ruthenium as catalysts for transfer hydrogenation
    • M.J. Page, J. Wagler, B.A. Messerle, Pyridine-2,6-bis(thioether) (SNS) complexes of ruthenium as catalysts for transfer hydrogenation, Organometallics 29 (2010) 3790-3798.
    • (2010) Organometallics , vol.29 , pp. 3790-3798
    • Page, M.J.1    Wagler, J.2    Messerle, B.A.3
  • 21
    • 77951568876 scopus 로고    scopus 로고
    • Coordinatively diverse ortho-phosphinoaniline complexes of ruthenium and isolation of a putative intermediate in ketone transfer hydrogenation catalysis
    • L.J. Hounjet, M. Bierenstiel, M.J. Ferguson, R. McDonald, M. Cowie, Coordinatively diverse ortho-phosphinoaniline complexes of ruthenium and isolation of a putative intermediate in ketone transfer hydrogenation catalysis, Inorg. Chem. 49 (2010) 4288-4300.
    • (2010) Inorg. Chem. , vol.49 , pp. 4288-4300
    • Hounjet, L.J.1    Bierenstiel, M.2    Ferguson, M.J.3    McDonald, R.4    Cowie, M.5
  • 23
    • 69249216340 scopus 로고    scopus 로고
    • Dicarbonylruthenium(II) complexes of diphosphine ligands and their catalytic activity
    • B. Deb, B.J. Borah, B.J. Sarmah, B. Das, D.K. Dutta, Dicarbonylruthenium(II) complexes of diphosphine ligands and their catalytic activity, Inorg. Chem. Commu. 12 (2009) 868-871.
    • (2009) Inorg. Chem. Commu. , vol.12 , pp. 868-871
    • Deb, B.1    Borah, B.J.2    Sarmah, B.J.3    Das, B.4    Dutta, D.K.5
  • 24
    • 79957626771 scopus 로고    scopus 로고
    • note
    • 2-RuS): C, 51.96 (51.72), H, 4.26 (4.24).
  • 25
    • 65249087271 scopus 로고    scopus 로고
    • Classical and weak hydrogen bonding interactions between 4,4′-bipyridine and organic acids: From co-crystal to organic complex
    • G.S. Nichol, W. Clegg, Classical and weak hydrogen bonding interactions between 4,4′-bipyridine and organic acids: from co-crystal to organic complex, Cryst. Growth. Des. 9 (2009) 1844-1850.
    • (2009) Cryst. Growth. Des. , vol.9 , pp. 1844-1850
    • Nichol, G.S.1    Clegg, W.2
  • 26
    • 25444435960 scopus 로고    scopus 로고
    • Strong and weak hydrogen-bonding interactions in the structures of N,N′,N′-trisubstituted guanidinium chlorides and bromides
    • DOI 10.1021/cg050172d
    • F.F. Said, T.G. Ong, G.P.A. Yap, D. Richeson, Strong and weak hydrogen-bonding interactions in the structures of n,n′,n″- trisubstitutedguanidinium chlorides and bromides, Cryst. Growth. Des. 5 (2005) 1881-1888. (Pubitemid 41362468)
    • (2005) Crystal Growth and Design , vol.5 , Issue.5 , pp. 1881-1888
    • Said, F.F.1    Ong, T.-G.2    Yap, G.P.A.3    Richeson, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.