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Volumn 47, Issue 20, 2008, Pages 3777-3780

Enantioselective copper-catalyzed propargylic amination

Author keywords

Amination; Asymmetricc atalysis; P,N ligands; Propargylic amines; Pybox ligands

Indexed keywords

AMINATION; AMINES; CHEMICAL REACTIONS; COPPER; LIGANDS; ORGANIC COMPOUNDS;

EID: 45549088523     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705264     Document Type: Article
Times cited : (199)

References (24)
  • 1
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    • Zani, L.1    Bolm, C.2
  • 2
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    • For a review, see
    • For a review, see: B. J. Teobald, Tetrahedron 2002, 58, 4133-4170.
    • (2002) Tetrahedron , vol.58 , pp. 4133-4170
    • Teobald, B.J.1
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    • Angew. Chem. Int. Ed. 2006, 45, 4970-4972;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 4970-4972
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    • Angew. Chem. Int. Ed. 2005, 44, 7715-7717.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 7715-7717
  • 15
    • 20344406206 scopus 로고    scopus 로고
    • for a selection of reported copper-pybox catalysts, see: b
    • for a selection of reported copper-pybox catalysts, see: b) J. Meng, V. V. Fokin, M. G. Finn, Tetrahedron Lett. 2005, 46, 4543-4546;
    • (2005) Tetrahedron Lett , vol.46 , pp. 4543-4546
    • Meng, J.1    Fokin, V.V.2    Finn, M.G.3
  • 19
    • 0141744680 scopus 로고    scopus 로고
    • The oxidative removal of the o-anisidyl group is well documented: J. F. Traverse, A. H. Hoveyda, M. L. Snapper, Org. Lett. 2003, 5, 3273-3275.
    • The oxidative removal of the o-anisidyl group is well documented: J. F. Traverse, A. H. Hoveyda, M. L. Snapper, Org. Lett. 2003, 5, 3273-3275.
  • 21
    • 0035905168 scopus 로고    scopus 로고
    • G. Desimoni, G. Faita, S. Filippone, M. Mella, M. G. Zampori, M. Zema, Tetrahedron 2001, 57, 10203-10212. When the other enantiomer of the pybox ligand (i.e. ent-6) was used, the reaction provided access to the opposite enantiomer of product 10a.
    • b) G. Desimoni, G. Faita, S. Filippone, M. Mella, M. G. Zampori, M. Zema, Tetrahedron 2001, 57, 10203-10212. When the other enantiomer of the pybox ligand (i.e. ent-6) was used, the reaction provided access to the opposite enantiomer of product 10a.
  • 22
    • 53549133435 scopus 로고    scopus 로고
    • More details of the optimization study can be found in Table 1 of the Supporting Information.
    • More details of the optimization study can be found in Table 1 of the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.