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Volumn 687, Issue 2, 2003, Pages 508-517

New chiral diamide ligands containing redox-active hydroquinone groups. Synthesis and results in the palladium(II)-catalyzed 1,4-diacetoxylation of 1,3-dienes

Author keywords

Asymmetric catalysis; Dienes; Ligand design; Oxidation; Palladium

Indexed keywords

ALKADIENE; BENZOIC ACID DERIVATIVE; BENZOQUINONE; BENZOYL PEROXIDE; DIAMIDE; HYDROQUINONE; LIGAND; PALLADIUM;

EID: 0344012068     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2003.09.007     Document Type: Article
Times cited : (22)

References (41)
  • 2
    • 0037990209 scopus 로고    scopus 로고
    • Palladium-catalyzed 1,4-additions to conjugated dienes
    • P. Stang, & F. Diederich (Eds.), Weinheim: Wiley-VCH
    • Bäckvall J.-E. Palladium-catalyzed 1,4-additions to conjugated dienes in: Stang P. Diederich F. (Eds.), Metal-Catalyzed Cross Coupling Reactions 1998 339-385 Wiley-VCH Weinheim
    • (1998) Metal-Catalyzed Cross Coupling Reactions , pp. 339-385
    • Bäckvall, J.-E.1
  • 27
    • 0345152415 scopus 로고    scopus 로고
    • A slower reaction usually leads to lower yields due to aromatisation as a side-reaction. The choice for this particular aromatisation-sensitive substrate is explained by the ease of separation on chiral HPLC
    • A slower reaction usually leads to lower yields due to aromatisation as a side-reaction. The choice for this particular aromatisation-sensitive substrate is explained by the ease of separation on chiral HPLC.
  • 34
    • 0345152414 scopus 로고    scopus 로고
    • A lower diastereoselectivity is not surprising, since higher acetate concentrations will favour the formation of the cis-addition product
    • A lower diastereoselectivity is not surprising, since higher acetate concentrations will favour the formation of the cis-addition product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.