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Volumn 16, Issue 3, 2005, Pages 609-614

Polymer-supported chiral phosphinooxathiane ligands for palladium-catalyzed asymmetric allylations

Author keywords

[No Author keywords available]

Indexed keywords

ALKANE DERIVATIVE; ALLYL COMPOUND; LIGAND; PALLADIUM; PHOSPHINE DERIVATIVE; POLYMER;

EID: 13844266763     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2004.11.090     Document Type: Article
Times cited : (35)

References (32)
  • 3
    • 0003544583 scopus 로고
    • I. Ojima VCH Weinheim
    • For a recent review on asymmetric allylic substitution, see: T. Hayashi I. Ojima Catalytic Asymmetric Synthesis 1993 VCH Weinheim 325
    • (1993) Catalytic Asymmetric Synthesis , pp. 325
    • Hayashi, T.1
  • 18
    • 0141631843 scopus 로고    scopus 로고
    • For some recent successful publications on polymer-supported chiral ligands in Pd-catalyzed allylic alkylation and amination: S.J. Greenfield, A. Agarkov, and S.R. Gilbertson Org. Lett. 5 2003 3069
    • (2003) Org. Lett. , vol.5 , pp. 3069
    • Greenfield, S.J.1    Agarkov, A.2    Gilbertson, S.R.3
  • 30
    • 85030824779 scopus 로고    scopus 로고
    • note
    • The conversions and loading efficiencies of 2a-c were calculated from the difference of the weights of the resins (PS-DES-Cl, PS-Et-COOH, and TentaGel-COOH) before the reactions, and those weights of the reactant resins after the reactions. The chemical yields of 2a-c were calculated based on the theoretical yields


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.