메뉴 건너뛰기




Volumn , Issue 24, 1998, Pages 2765-2766

Enantioselective palladium catalyzed allylic substitution with chiral thioether derivatives of ferrocenyl-oxazoline and the role of planar chirality in this reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; LIGAND; OXAZOLIDINE DERIVATIVE; PALLADIUM; SULFIDE;

EID: 0032556757     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a808267g     Document Type: Article
Times cited : (101)

References (25)
  • 1
    • 0026722772 scopus 로고
    • Reviews: C. G. Frost, J. Howarth and J. M. J. Williams, Tetrahedron: Asymmetry, 1992, 3, 1089; B. M. Trost and D. L. Van Vranken, Chem. Rev., 1996, 96, 395; G. Consiglio and R. M. Waymouth, Chem. Rev., 1989, 89, 257; S. A. Godleski, in Comprehensive Organic Synthesis, ed. B. H. Trost, Pergamon Press, Oxford, 1991, vol. 4. p. 585.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 1089
    • Frost, C.G.1    Howarth, J.2    Williams, J.M.J.3
  • 2
    • 6844254916 scopus 로고    scopus 로고
    • Reviews: C. G. Frost, J. Howarth and J. M. J. Williams, Tetrahedron: Asymmetry, 1992, 3, 1089; B. M. Trost and D. L. Van Vranken, Chem. Rev., 1996, 96, 395; G. Consiglio and R. M. Waymouth, Chem. Rev., 1989, 89, 257; S. A. Godleski, in Comprehensive Organic Synthesis, ed. B. H. Trost, Pergamon Press, Oxford, 1991, vol. 4. p. 585.
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 3
    • 0024302311 scopus 로고
    • Reviews: C. G. Frost, J. Howarth and J. M. J. Williams, Tetrahedron: Asymmetry, 1992, 3, 1089; B. M. Trost and D. L. Van Vranken, Chem. Rev., 1996, 96, 395; G. Consiglio and R. M. Waymouth, Chem. Rev., 1989, 89, 257; S. A. Godleski, in Comprehensive Organic Synthesis, ed. B. H. Trost, Pergamon Press, Oxford, 1991, vol. 4. p. 585.
    • (1989) Chem. Rev. , vol.89 , pp. 257
    • Consiglio, G.1    Waymouth, R.M.2
  • 4
    • 0000276556 scopus 로고
    • ed. B. H. Trost, Pergamon Press, Oxford
    • Reviews: C. G. Frost, J. Howarth and J. M. J. Williams, Tetrahedron: Asymmetry, 1992, 3, 1089; B. M. Trost and D. L. Van Vranken, Chem. Rev., 1996, 96, 395; G. Consiglio and R. M. Waymouth, Chem. Rev., 1989, 89, 257; S. A. Godleski, in Comprehensive Organic Synthesis, ed. B. H. Trost, Pergamon Press, Oxford, 1991, vol. 4. p. 585.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 585
    • Godleski, S.A.1
  • 5
    • 31544439675 scopus 로고    scopus 로고
    • Recent examples: B. M. Trost and R. C. Bunt, Angew. Chem. Int. Ed. Engl, 1996, 35, 99; B. M. Trost and F. D. Toste, J. Am. Chem. Soc., 1998, 120, 815; B. M. Trost and D. E. Patterson, J. Org. Chem., 1998, 63, 1339.
    • (1996) Angew. Chem. Int. Ed. Engl , vol.35 , pp. 99
    • Trost, B.M.1    Bunt, R.C.2
  • 6
    • 0032481394 scopus 로고    scopus 로고
    • Recent examples: B. M. Trost and R. C. Bunt, Angew. Chem. Int. Ed. Engl, 1996, 35, 99; B. M. Trost and F. D. Toste, J. Am. Chem. Soc., 1998, 120, 815; B. M. Trost and D. E. Patterson, J. Org. Chem., 1998, 63, 1339.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 815
    • Trost, B.M.1    Toste, F.D.2
  • 7
    • 31544439675 scopus 로고    scopus 로고
    • Recent examples: B. M. Trost and R. C. Bunt, Angew. Chem. Int. Ed. Engl, 1996, 35, 99; B. M. Trost and F. D. Toste, J. Am. Chem. Soc., 1998, 120, 815; B. M. Trost and D. E. Patterson, J. Org. Chem., 1998, 63, 1339.
    • (1998) J. Org. Chem. , vol.63 , pp. 1339
    • Trost, B.M.1    Patterson, D.E.2
  • 14
    • 0000565505 scopus 로고    scopus 로고
    • J. C. Ruble, J. Tweddell and G. C. Fu, J. Org. Chem., 1998, 63, 2794; S. Qiao and G. C. Fu, J. Org. Chem., 1998, 63, 4168.
    • (1998) J. Org. Chem. , vol.63 , pp. 4168
    • Qiao, S.1    Fu, G.C.2
  • 15
    • 0030024622 scopus 로고    scopus 로고
    • A. H. Li, L. X. Dai, X. L. Hou, Y. Z. Huang and F. W. Li, J. Org. Chem., 1996, 61, 489; A. H. Li, Y. G. Zhou, L. X. Dai, X. L. Hou, L. J. Xia and L. Lin, Angew. Chem., Int. Ed. Engl., 1997, 36, 1317.
    • (1996) J. Org. Chem. , vol.61 , pp. 489
    • Li, A.H.1    Dai, L.X.2    Hou, X.L.3    Huang, Y.Z.4    Li, F.W.5
  • 22
    • 0025096429 scopus 로고
    • A. M. Warshawsky and A. I. Meyers, J. Am. Chem. Soc., 1990, 112, 8090; T. D. Nelson and A. I. Meyers, J. Org. Chem., 1994, 59, 2655; W. B. Zhang, T. Kido, Y. Nakatsuji and I. Ikeda, Tetrahedron Lett., 1996, 37, 7995.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 8090
    • Warshawsky, A.M.1    Meyers, A.I.2
  • 23
    • 0001054255 scopus 로고
    • A. M. Warshawsky and A. I. Meyers, J. Am. Chem. Soc., 1990, 112, 8090; T. D. Nelson and A. I. Meyers, J. Org. Chem., 1994, 59, 2655; W. B. Zhang, T. Kido, Y. Nakatsuji and I. Ikeda, Tetrahedron Lett., 1996, 37, 7995.
    • (1994) J. Org. Chem. , vol.59 , pp. 2655
    • Nelson, T.D.1    Meyers, A.I.2
  • 24
    • 0030605145 scopus 로고    scopus 로고
    • A. M. Warshawsky and A. I. Meyers, J. Am. Chem. Soc., 1990, 112, 8090; T. D. Nelson and A. I. Meyers, J. Org. Chem., 1994, 59, 2655; W. B. Zhang, T. Kido, Y. Nakatsuji and I. Ikeda, Tetrahedron Lett., 1996, 37, 7995.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7995
    • Zhang, W.B.1    Kido, T.2    Nakatsuji, Y.3    Ikeda, I.4
  • 25
    • 0345220030 scopus 로고    scopus 로고
    • note
    • We also noticed a similar rate enhancing effect in the asymmetric transfer hydrogenation of ketones catalyzed by ruthenium complexes with phosphinoferrocenyloxozolines (ref. 6).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.