메뉴 건너뛰기




Volumn 5, Issue 4, 1999, Pages 1160-1165

Chiral 1,2-bis(phosphetano)benzenes: Preparation and use in the Ru- catalyzed hydrogenations of carbonyl derivatives

Author keywords

Catalysts; Chiral phosphetanes; Hydrogenations; Phosphorus; Ruthenium

Indexed keywords

BENZENE DERIVATIVE; RUTHENIUM COMPLEX;

EID: 0032947082     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(19990401)5:4<1160::AID-CHEM1160>3.0.CO;2-3     Document Type: Article
Times cited : (65)

References (32)
  • 1
    • 0000546172 scopus 로고
    • M. J. Burk, J. E. Feaster, R. L. Harlow, Organometallics 1990, 9, 2653; M. J. Burk, J. E. Feaster, W. A. Nugent, R. L. Harlow, J. Am. Chem. Soc. 1993, 115, 10125; for a recent review see: M. J. Burk, M. F. Gross, T. G. P. Harper, C. S. Kalherg, J. R. Lee, J. P. Martinez, Pure Appl. Chem. 1996, 68, 37.
    • (1990) Organometallics , vol.9 , pp. 2653
    • Burk, M.J.1    Feaster, J.E.2    Harlow, R.L.3
  • 2
    • 0000740766 scopus 로고
    • M. J. Burk, J. E. Feaster, R. L. Harlow, Organometallics 1990, 9, 2653; M. J. Burk, J. E. Feaster, W. A. Nugent, R. L. Harlow, J. Am. Chem. Soc. 1993, 115, 10125; for a recent review see: M. J. Burk, M. F. Gross, T. G. P. Harper, C. S. Kalherg, J. R. Lee, J. P. Martinez, Pure Appl. Chem. 1996, 68, 37.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10125
    • Burk, M.J.1    Feaster, J.E.2    Nugent, W.A.3    Harlow, R.L.4
  • 5
    • 0032482106 scopus 로고    scopus 로고
    • Q. Jiang, Y. Jiang, D. Xiao, P. Cao, X. Zhang, Angew. Chem. 1998, 110, 1203; Angew. Chem. Int. Ed. 1998, 37, 1100.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1100
  • 7
    • 0000670009 scopus 로고    scopus 로고
    • 1-Phenylphosphetane rapidly polymerizes: D. C. R. Hockless, Y. B. Kang, M. A. McDonald, M. Pabel, A. Willis, S. B. Wild. Organometallics 1996, 75, 1301; while C-substituted species display high thermal stability, as shown by a number of literature reports: T. Kawashima, R. Okazaki in Comprehensive Heterocyclic Chemistry II, Vol. 1 (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon, 1996, p. 833, and references therein.
    • (1996) Organometallics , vol.75 , pp. 1301
    • Hockless, D.C.R.1    Kang, Y.B.2    McDonald, M.A.3    Pabel, M.4    Willis, A.5    Wild, S.B.6
  • 8
    • 0003607021 scopus 로고    scopus 로고
    • (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon
    • 1-Phenylphosphetane rapidly polymerizes: D. C. R. Hockless, Y. B. Kang, M. A. McDonald, M. Pabel, A. Willis, S. B. Wild. Organometallics 1996, 75, 1301; while C-substituted species display high thermal stability, as shown by a number of literature reports: T. Kawashima, R. Okazaki in Comprehensive Heterocyclic Chemistry II, Vol. 1 (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon, 1996, p. 833, and references therein.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.1 , pp. 833
    • Kawashima, T.1    Okazaki, R.2
  • 9
    • 0000948481 scopus 로고
    • Little is known about the catalytic behaviour of chiral phosphetanes. Only highly substituted, hindered species have been used in palladium-promoted reactions: A. Marinetti, L. Ricard, Organometallics 1994, 13, 3956; A. Marinetti, V. Kruger, L. Ricard, J. Organomet. Chem. 1997, 529, 465.
    • (1994) Organometallics , vol.13 , pp. 3956
    • Marinetti, A.1    Ricard, L.2
  • 10
    • 0031568647 scopus 로고    scopus 로고
    • Little is known about the catalytic behaviour of chiral phosphetanes. Only highly substituted, hindered species have been used in palladium-promoted reactions: A. Marinetti, L. Ricard, Organometallics 1994, 13, 3956; A. Marinetti, V. Kruger, L. Ricard, J. Organomet. Chem. 1997, 529, 465.
    • (1997) J. Organomet. Chem. , vol.529 , pp. 465
    • Marinetti, A.1    Kruger, V.2    Ricard, L.3
  • 12
    • 0030846119 scopus 로고    scopus 로고
    • J.-P. Genêt, C. Pinel, V. Ratovelomanana-Vidal, S. Mallart, X. Pfister, L. Bischoff, M. C. Caño De Andrade, S. Darses, C. Galopin, J. A. Laffitte, Tetrahedron: Asymmetry 1994, 5, 675; D. Blanc. J. C. Henry, V. Ratovelomanana-Vidal, J.-P. Genêt. Tetrahedron Lett. 1997, 38, 6603; for recent reviews see: J.-P. Genêt in Reductions in Organic Synthesis (Ed.: A. F. Abdel Magid), A. C. S. Symposium Series 641, 1996, pp. 31-51; J.-P. Genêt, in Advances in Asymmetric Synthesis (Ed.: G. R. Stephenson), Chapman and Hall, London, 1996, pp. 60-92.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6603
    • Blanc, D.1    Henry, J.C.2    Ratovelomanana-Vidal, V.3    Genêt, J.-P.4
  • 13
    • 1542680893 scopus 로고    scopus 로고
    • Reductions in organic synthesis
    • (Ed.: A. F. Abdel Magid)
    • J.-P. Genêt, C. Pinel, V. Ratovelomanana-Vidal, S. Mallart, X. Pfister, L. Bischoff, M. C. Caño De Andrade, S. Darses, C. Galopin, J. A. Laffitte, Tetrahedron: Asymmetry 1994, 5, 675; D. Blanc. J. C. Henry, V. Ratovelomanana-Vidal, J.-P. Genêt. Tetrahedron Lett. 1997, 38, 6603; for recent reviews see: J.-P. Genêt in Reductions in Organic Synthesis (Ed.: A. F. Abdel Magid), A. C. S. Symposium Series 641, 1996, pp. 31-51; J.-P. Genêt, in Advances in Asymmetric Synthesis (Ed.: G. R. Stephenson), Chapman and Hall, London, 1996, pp. 60-92.
    • (1996) A. C. S. Symposium Series , vol.641 , pp. 31-51
    • Genêt, J.-P.1
  • 14
    • 0002025802 scopus 로고    scopus 로고
    • (Ed.: G. R. Stephenson), Chapman and Hall, London
    • J.-P. Genêt, C. Pinel, V. Ratovelomanana-Vidal, S. Mallart, X. Pfister, L. Bischoff, M. C. Caño De Andrade, S. Darses, C. Galopin, J. A. Laffitte, Tetrahedron: Asymmetry 1994, 5, 675; D. Blanc. J. C. Henry, V. Ratovelomanana-Vidal, J.-P. Genêt. Tetrahedron Lett. 1997, 38, 6603; for recent reviews see: J.-P. Genêt in Reductions in Organic Synthesis (Ed.: A. F. Abdel Magid), A. C. S. Symposium Series 641, 1996, pp. 31-51; J.-P. Genêt, in Advances in Asymmetric Synthesis (Ed.: G. R. Stephenson), Chapman and Hall, London, 1996, pp. 60-92.
    • (1996) Advances in Asymmetric Synthesis , pp. 60-92
    • Genêt, J.-P.1
  • 22
    • 0028898315 scopus 로고
    • 4/L-(+)-diisopropyl tartrate-catalyzed Sharpless epoxidation of 2,6-dimethyl-4-hepten-3-ol: C. Jacoby, J. C. Braekman, D. Daloze, Tetrahedron: Asymmetry 1995, 6, 753; or by hydrogenation over Raney Nickel modified with tartaric acid: T. Sugimura, M. Yoshikawa, T. Yoneda, A. Tai, Bull. Chem. Soc. Jpn. 1990, 63, 1080; A. Tai, T. Kikukawa, T. Sugimura, Y. Inoue, T. Osawa, S. Fujii, J. Chem. Soc. Chem. Commun. 1991, 795.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 753
    • Jacoby, C.1    Braekman, J.C.2    Daloze, D.3
  • 23
    • 0025040887 scopus 로고
    • 4/L-(+)-diisopropyl tartrate-catalyzed Sharpless epoxidation of 2,6-dimethyl-4-hepten-3-ol: C. Jacoby, J. C. Braekman, D. Daloze, Tetrahedron: Asymmetry 1995, 6, 753; or by hydrogenation over Raney Nickel modified with tartaric acid: T. Sugimura, M. Yoshikawa, T. Yoneda, A. Tai, Bull. Chem. Soc. Jpn. 1990, 63, 1080; A. Tai, T. Kikukawa, T. Sugimura, Y. Inoue, T. Osawa, S. Fujii, J. Chem. Soc. Chem. Commun. 1991, 795.
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 1080
    • Sugimura, T.1    Yoshikawa, M.2    Yoneda, T.3    Tai, A.4
  • 24
    • 84942718931 scopus 로고
    • 4/L-(+)-diisopropyl tartrate-catalyzed Sharpless epoxidation of 2,6-dimethyl-4-hepten-3-ol: C. Jacoby, J. C. Braekman, D. Daloze, Tetrahedron: Asymmetry 1995, 6, 753; or by hydrogenation over Raney Nickel modified with tartaric acid: T. Sugimura, M. Yoshikawa, T. Yoneda, A. Tai, Bull. Chem. Soc. Jpn. 1990, 63, 1080; A. Tai, T. Kikukawa, T. Sugimura, Y. Inoue, T. Osawa, S. Fujii, J. Chem. Soc. Chem. Commun. 1991, 795.
    • (1991) J. Chem. Soc. Chem. Commun. , pp. 795
    • Tai, A.1    Kikukawa, T.2    Sugimura, T.3    Inoue, Y.4    Osawa, T.5    Fujii, S.6
  • 25
    • 0344954820 scopus 로고    scopus 로고
    • (Chiroscience Ltd.), WO 98/02445
    • U. Berens (Chiroscience Ltd.), WO 98/02445, 1998.
    • (1998)
    • Berens, U.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.