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Volumn 129, Issue 11, 2007, Pages 3076-3077

Palladium(II)-catalyzed enantioselective aerobic dialkoxylation of 2-propenyl phenols: A pronounced effect of copper additives on enantioselectivity

Author keywords

[No Author keywords available]

Indexed keywords

2 PROPENYLPHENOL; COPPER; LIGAND; OXAZOLINE DERIVATIVE; PALLADIUM; PHENOL DERIVATIVE; QUINOLINE DERIVATIVE; QUINONE DERIVATIVE; SPARTEINE; STYRENE; UNCLASSIFIED DRUG;

EID: 33947407602     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja070263u     Document Type: Article
Times cited : (221)

References (18)
  • 1
    • 4043123499 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Tietze, L. F.; Ila, H.; Bell, H. P. Chem. Rev. 2004, 104, 3453-3516.
    • (2004) Chem. Rev , vol.104 , pp. 3453-3516
    • Tietze, L.F.1    Ila, H.2    Bell, H.P.3
  • 2
    • 0003441482 scopus 로고
    • Tsuji, J, Ed, Wiley: Chichester, U.K
    • (b) Palladium Reagents and Catalysis; Tsuji, J., Ed.; Wiley: Chichester, U.K., 1995.
    • (1995) Palladium Reagents and Catalysis
  • 3
    • 0037102993 scopus 로고    scopus 로고
    • For examples of intermolecular enantioselective nucleopalladation, see: (a) El-Qisairi, A. K, Qaseer, H. A, Henry, P. M. J. Organomet. Chem. 2002, 656, 168-176
    • For examples of intermolecular enantioselective nucleopalladation, see: (a) El-Qisairi, A. K.; Qaseer, H. A.; Henry, P. M. J. Organomet. Chem. 2002, 656, 168-176.
  • 14
    • 33947381621 scopus 로고    scopus 로고
    • Catalyst decomposition was observed
    • Catalyst decomposition was observed.
  • 15
    • 4444357128 scopus 로고    scopus 로고
    • For recent enantioselective reactions utilizing chiral quinoline oxazolines, see: a
    • For recent enantioselective reactions utilizing chiral quinoline oxazolines, see: (a) Abrunhosa, I.; Bioton, L.; Gaumount, A.; Gulea, M.; Masson, S. Tetrahedron 2004, 60, 9263.
    • (2004) Tetrahedron , vol.60 , pp. 9263
    • Abrunhosa, I.1    Bioton, L.2    Gaumount, A.3    Gulea, M.4    Masson, S.5
  • 17
    • 33749828310 scopus 로고    scopus 로고
    • For a recent review of oxazoline synthetic methods, see
    • For a recent review of oxazoline synthetic methods, see: Desimoni, G.; Faita, G.; Jorgensen, K. A. Chem. Rev. 2006, 106, 3561-3651.
    • (2006) Chem. Rev , vol.106 , pp. 3561-3651
    • Desimoni, G.1    Faita, G.2    Jorgensen, K.A.3
  • 18
    • 33947431397 scopus 로고    scopus 로고
    • The absolute configuration of the product was determined by comparison to an independently prepared authentic sample. See Supporting Information for details
    • The absolute configuration of the product was determined by comparison to an independently prepared authentic sample. See Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.