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Volumn , Issue 1, 2004, Pages 106-110

The Application of HETPHOX Ligands to the Asymmetric Intermolecular Heck Reaction

Author keywords

Asymmetric catalysis; Intermolecular Heck reaction; Oxazoline; P,N ligands; Palladium

Indexed keywords

2,3 DIHYDRO 2 PHENYLFURAN; 2,3 DIHYDROFURAN; BENZOTHIOPHENE; FURAN DERIVATIVE; LIGAND; OXAZOLINE DERIVATIVE; THIOPHENE; UNCLASSIFIED DRUG;

EID: 0348231765     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-43345     Document Type: Article
Times cited : (32)

References (38)
  • 1
    • 0004136293 scopus 로고
    • For extensive reviews of the Heck reaction see: (a) Heck, R. F. Acc. Chem. Res. 1979, 146. (b) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 28, 2379. (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (d) Guiry, P. J.; Hennessy, A. J.; Cahill, J. P. Top. Catal. 1997, 4, 311. (e) Jeffrey, T. Advances in Metal-Organic Chemistry, Vol 5; JAI Press Inc.: Conneticut, 1996, 153.
    • (1979) Acc. Chem. Res. , pp. 146
    • Heck, R.F.1
  • 2
    • 0001217660 scopus 로고
    • For extensive reviews of the Heck reaction see: (a) Heck, R. F. Acc. Chem. Res. 1979, 146. (b) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 28, 2379. (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (d) Guiry, P. J.; Hennessy, A. J.; Cahill, J. P. Top. Catal. 1997, 4, 311. (e) Jeffrey, T. Advances in Metal-Organic Chemistry, Vol 5; JAI Press Inc.: Conneticut, 1996, 153.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.28 , pp. 2379
    • De Meijere, A.1    Meyer, F.E.2
  • 3
    • 0038584673 scopus 로고
    • For extensive reviews of the Heck reaction see: (a) Heck, R. F. Acc. Chem. Res. 1979, 146. (b) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 28, 2379. (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (d) Guiry, P. J.; Hennessy, A. J.; Cahill, J. P. Top. Catal. 1997, 4, 311. (e) Jeffrey, T. Advances in Metal-Organic Chemistry, Vol 5; JAI Press Inc.: Conneticut, 1996, 153.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 2
    • Cabri, W.1    Candiani, I.2
  • 4
    • 0001423916 scopus 로고    scopus 로고
    • For extensive reviews of the Heck reaction see: (a) Heck, R. F. Acc. Chem. Res. 1979, 146. (b) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 28, 2379. (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (d) Guiry, P. J.; Hennessy, A. J.; Cahill, J. P. Top. Catal. 1997, 4, 311. (e) Jeffrey, T. Advances in Metal-Organic Chemistry, Vol 5; JAI Press Inc.: Conneticut, 1996, 153.
    • (1997) Top. Catal. , vol.4 , pp. 311
    • Guiry, P.J.1    Hennessy, A.J.2    Cahill, J.P.3
  • 5
    • 0000629440 scopus 로고    scopus 로고
    • JAI Press Inc.: Conneticut
    • For extensive reviews of the Heck reaction see: (a) Heck, R. F. Acc. Chem. Res. 1979, 146. (b) De Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 28, 2379. (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2. (d) Guiry, P. J.; Hennessy, A. J.; Cahill, J. P. Top. Catal. 1997, 4, 311. (e) Jeffrey, T. Advances in Metal-Organic Chemistry, Vol 5; JAI Press Inc.: Conneticut, 1996, 153.
    • (1996) Advances in Metal-Organic Chemistry , vol.5 , pp. 153
    • Jeffrey, T.1
  • 33
    • 0348055791 scopus 로고    scopus 로고
    • note
    • +], 364 (4), 336 (19), 308 (100), 288 (53), 234 (9) and 89 (18).
  • 37
    • 0348055790 scopus 로고    scopus 로고
    • note
    • 2O (10 mL). This solution was then concentrated and the yield calculated using GC (Se-30, 11 psi, 50°C, 4 min, 15°C/min, 170°C, 10 min) by the internal standard method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.