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Volumn 42, Issue 39, 2003, Pages 4789-4792

CuH-Catalyzed Asymmetric Conjugate Reductions of Acyclic Enones

Author keywords

Conjugate reductions; Copper hydride; Enones; Hydrosilylation; Phosphane ligands

Indexed keywords

CATALYSIS; REDUCTION; STOICHIOMETRY;

EID: 0142183577     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352313     Document Type: Article
Times cited : (149)

References (45)
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    • M. Shibasaki, H. Sasai, T. Arai, Angew. Chem. 1997, 109, 1290; Angew. Chem. Int. Ed. Engl. 1997, 36, 1236.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1236
  • 21
    • 0011040448 scopus 로고
    • Due to the tack of any suitable means of effecting such asymmetric conjugate reductions, this strategy is usually not even considered an option for the control of stereochemistry at a site β to a ketone.[1] For early hydrogenation studies on enones using nonracemic ruthenium and cobalt complexes, see V. Massonneau, P. Le Maux, G. Simonneaux, J. Organomet. Chem. 1987, 327, 269; P. Le Maux, V. Massonneau, G. Simonneaux, J. Organomet. Chem. 1985, 284, 101.
    • (1987) J. Organomet. Chem. , vol.327 , pp. 269
    • Massonneau, V.1    Le Maux, P.2    Simonneaux, G.3
  • 22
    • 0142214972 scopus 로고
    • Due to the tack of any suitable means of effecting such asymmetric conjugate reductions, this strategy is usually not even considered an option for the control of stereochemistry at a site β to a ketone.[1] For early hydrogenation studies on enones using nonracemic ruthenium and cobalt complexes, see V. Massonneau, P. Le Maux, G. Simonneaux, J. Organomet. Chem. 1987, 327, 269; P. Le Maux, V. Massonneau, G. Simonneaux, J. Organomet. Chem. 1985, 284, 101.
    • (1985) J. Organomet. Chem. , vol.284 , pp. 101
    • Le Maux, P.1    Massonneau, V.2    Simonneaux, G.3
  • 40
    • 0142152776 scopus 로고
    • 3), whereas R-9 gave an equal and opposite (positive) rotation, as expected for these known compounds; cf. G. Bram, D. Caberet, N. Maigrot, J.-P. Mazaleyrat, Z. Welvart, J. Chem. Res. Synop. 1979, 196; D. Caberet, N. Maigrot, Z. Welvart, Tetrahedron Lett. 1981, 22, 5279.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 5279
    • Caberet, D.1    Maigrot, N.2    Welvart, Z.3
  • 43
    • 0142214969 scopus 로고    scopus 로고
    • note
    • 9: 215.1467; found 215.1470. Additional data for all new compounds can be found in the Supporting Information.
  • 45
    • 0037011208 scopus 로고    scopus 로고
    • B. H. Lipshutz, P. Papa, Angew. Chem. 2002, 114, 4762; Angew. Chem. Int. Ed. 2002, 41, 4580.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4580


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.