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Volumn 23, Issue 11-12, 2012, Pages 859-866

Enantioselective construction of all-carbon quaternary spirocenters through a Pd-catalyzed asymmetric intramolecular ipso-Friedel-Crafts allylic alkylation of phenols

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; PHENOL DERIVATIVE;

EID: 84864211395     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2012.05.026     Document Type: Article
Times cited : (83)

References (74)
  • 25
    • 0032481394 scopus 로고    scopus 로고
    • For an example of a Pd-catalyzed C-allylation of phenols via an O-allylation-Claisen rearrangement sequence, see: B.M. Trost, and F.D. Toste J. Am. Chem. Soc. 120 1998 815
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 815
    • Trost, B.M.1    Toste, F.D.2
  • 27
    • 0035905575 scopus 로고    scopus 로고
    • For reviews on the catalytic asymmetric construction of quaternary stereocenters, see: J. Christoffers, and A. Mann Angew. Chem., Int. Ed. 40 2001 4591
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4591
    • Christoffers, J.1    Mann, A.2
  • 56
    • 0033947876 scopus 로고    scopus 로고
    • For a review on MOP ligands, see: T. Hayashi Acc. Chem. Res. 33 2000 354
    • (2000) Acc. Chem. Res. , vol.33 , pp. 354
    • Hayashi, T.1
  • 63
    • 0034639986 scopus 로고    scopus 로고
    • For recent selected examples of catalytic asymmetric reactions using the Trost ligand 3k, see: B.M. Trost, H.-C. Tsui, and F.D. Toste J. Am. Chem. Soc. 122 2000 3534
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 3534
    • Trost, B.M.1    Tsui, H.-C.2    Toste, F.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.