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Volumn 603, Issue 1, 2000, Pages 40-49

Palladium-catalyzed asymmetric intermolecular arylation of cyclic or acyclic alkenes using phosphinite-oxazoline ligands derived from D-glucosamine

Author keywords

Asymmetric catalysis; D Glucosamine; Intermolecular arylation; Phosphinite oxazoline ligand

Indexed keywords


EID: 0003002302     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00069-3     Document Type: Article
Times cited : (75)

References (50)
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    • For recent overviews, see for example: (a) M. Shibasaki, E.M. Vogl, J. Organomet. Chem. 576 (1999) 1. (b) O. Loiseleur, M. Hayashi, M. Keenan, N. Schmees, A. Pfaltz, J. Organomet. Chem. 576 (1999) 16. (c) M. Shibasaki, C.D.J. Boden, A. Kojima, Tetrahedron 53 (1997) 7371.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 1
    • Shibasaki, M.1    Vogl, E.M.2
  • 3
    • 0001913446 scopus 로고    scopus 로고
    • For recent overviews, see for example: (a) M. Shibasaki, E.M. Vogl, J. Organomet. Chem. 576 (1999) 1. (b) O. Loiseleur, M. Hayashi, M. Keenan, N. Schmees, A. Pfaltz, J. Organomet. Chem. 576 (1999) 16. (c) M. Shibasaki, C.D.J. Boden, A. Kojima, Tetrahedron 53 (1997) 7371.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 16
    • Loiseleur, O.1    Hayashi, M.2    Keenan, M.3    Schmees, N.4    Pfaltz, A.5
  • 4
    • 0030995738 scopus 로고    scopus 로고
    • For recent overviews, see for example: (a) M. Shibasaki, E.M. Vogl, J. Organomet. Chem. 576 (1999) 1. (b) O. Loiseleur, M. Hayashi, M. Keenan, N. Schmees, A. Pfaltz, J. Organomet. Chem. 576 (1999) 16. (c) M. Shibasaki, C.D.J. Boden, A. Kojima, Tetrahedron 53 (1997) 7371.
    • (1997) Tetrahedron , vol.53 , pp. 7371
    • Shibasaki, M.1    Boden, C.D.J.2    Kojima, A.3
  • 28
    • 0030743672 scopus 로고    scopus 로고
    • On the mechanism of the catalysis involving diphosphines, see: (a) C. Amatore, G. Broeker, A. Jutand, F. Khalil, J. Am. Chem. Soc. 119 (1997) 5176. (b) K.K. (Mimi) Hu, T.D.W. Claridge, J.M. Brown, Angew. Chem., Int. Ed. Engl. 36 (1997) 984.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 5176
    • Amatore, C.1    Broeker, G.2    Jutand, A.3    Khalil, F.4
  • 29
    • 0005864080 scopus 로고    scopus 로고
    • On the mechanism of the catalysis involving diphosphines, see: (a) C. Amatore, G. Broeker, A. Jutand, F. Khalil, J. Am. Chem. Soc. 119 (1997) 5176. (b) K.K. (Mimi) Hu, T.D.W. Claridge, J.M. Brown, Angew. Chem., Int. Ed. Engl. 36 (1997) 984.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 984
    • Hu, K.K.1    Claridge, T.D.W.2    Brown, J.M.3
  • 36
    • 85037490440 scopus 로고    scopus 로고
    • Mizoroki-Heck-type reaction of chiral but-3-en-2-ol and pent-3-en-2-ol has been reported in Ref. [9b]
    • Mizoroki-Heck-type reaction of chiral but-3-en-2-ol and pent-3-en-2-ol has been reported in Ref. [9b].
  • 41
    • 85037455739 scopus 로고    scopus 로고
    • note
    • 2 in their molecules as shown in experimental section.
  • 42
    • 85037466378 scopus 로고    scopus 로고
    • note
    • No coupling (J = O Hz) was observed between the phosphorus and ipso-carbon in both complexes 8 and 9. The larger coupling constants over 100 Hz between a phosphorus nucleus and trans ipso-carbon of related complexes have been reported [6d].
  • 43
    • 85037468525 scopus 로고    scopus 로고
    • note
    • 13C-NMR spectrum of 11 showed the coupling constant (J = 2.0 Hz) between a phosphorus and an ipso-carbon.
  • 44
    • 85037462825 scopus 로고    scopus 로고
    • note
    • No peak of a hydride was also observed through the range from - 100 to 0 ppm.
  • 47
    • 85037459555 scopus 로고    scopus 로고
    • TEXSAN: crystal structure analysis package, molecular structure, 1985 and 1992
    • TEXSAN: crystal structure analysis package, molecular structure, 1985 and 1992.
  • 50
    • 0000191360 scopus 로고
    • A.J.C. Wilson (Ed.), Kluwer Academic Publishers, Boston, Tables 4.2, 4.3
    • D.C. Creagh, J.H. Hubbell, in: A.J.C. Wilson (Ed.), International Tables for Crystallography, vol. C, Kluwer Academic Publishers, Boston, 1992, Tables 4.2, 4.3, pp. 200-206.
    • (1992) International Tables for Crystallography , vol.100 , pp. 200-206
    • Creagh, D.C.1    Hubbell, J.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.