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Volumn 48, Issue 19, 2007, Pages 3389-3391

Asymmetric construction of quaternary carbon stereocenter by Pd-hemilabile ligand-catalyzed allylic substitution

Author keywords

Asymmetric quaternary carbon; Chiral hemilabile ligand; Enantioselective Pd catalyzed allylic substitution

Indexed keywords

1',2 BIS(DIPHENYLPHOSPHINOETHYL)FERROCENYL ALCOHOL; CARBON; CYCLOHEXANONE DERIVATIVE; FERROCENE DERIVATIVE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 34147121378     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.03.065     Document Type: Article
Times cited : (16)

References (31)
  • 8
    • 0035804417 scopus 로고    scopus 로고
    • For the definition of hemilabile ligands, see:
    • For the definition of hemilabile ligands, see:. Braunstein P., and Naud F. Angew. Chem., Int. Ed. 40 (2001) 680-699
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 680-699
    • Braunstein, P.1    Naud, F.2
  • 15
    • 0030567369 scopus 로고    scopus 로고
    • For successful examples (>90% ee), see:
    • For successful examples (>90% ee), see:. Sawamura M., Sudoh M., and Ito Y. J. Am. Chem. Soc. 118 (1996) 3309-3310
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 3309-3310
    • Sawamura, M.1    Sudoh, M.2    Ito, Y.3
  • 19
    • 34147120889 scopus 로고    scopus 로고
    • note
    • Ligand 5, 8, and 9 are new compounds.
  • 20
    • 0042250061 scopus 로고
    • For a review, see:
    • For a review, see:. Sawamura M., and Ito Y. Chem. Rev. 92 (1992) 857-871
    • (1992) Chem. Rev. , vol.92 , pp. 857-871
    • Sawamura, M.1    Ito, Y.2
  • 26
    • 34147112005 scopus 로고    scopus 로고
    • For successful examples, see: Ref. 7.
  • 28
    • 0001327455 scopus 로고
    • The Pd-10-catalyzed asymmetric allylic alkylation of allylacetate with β-diketone has been reported by Hayashi, but the enantioselectivity was 30%:
    • The Pd-10-catalyzed asymmetric allylic alkylation of allylacetate with β-diketone has been reported by Hayashi, but the enantioselectivity was 30%:. Hayashi T., Kanehira K., Hagihara T., and Kumada M. J. Org. Chem. 53 (1988) 113-120
    • (1988) J. Org. Chem. , vol.53 , pp. 113-120
    • Hayashi, T.1    Kanehira, K.2    Hagihara, T.3    Kumada, M.4
  • 29
    • 33846192045 scopus 로고    scopus 로고
    • For successful examples of constructing a quaternary carbon stereo center by other asymmetric allylic alkylations:
    • For successful examples of constructing a quaternary carbon stereo center by other asymmetric allylic alkylations:. Trost B.M., Xu J., and Reichle M. J. Am. Chem. Soc. 129 (2007) 282-283
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 282-283
    • Trost, B.M.1    Xu, J.2    Reichle, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.