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Volumn 49, Issue 48, 2008, Pages 6924-6928

Cyclization-oxidation of 1,6-enyne derivatived from Baylis-Hillman adducts via Pd(II)/Pd(IV)-catalyzed reactions: stereoselective synthesis of multi-substituted bicyclo[3.1.0] hexanes and insight into reaction pathways

Author keywords

Baylis Hillman adduct; Bicyclo 3.1.0 ; C C bond formation; Cyclization oxidation; SN2 type reductive elimination

Indexed keywords

BICYCLO COMPOUND; CARBON; HEXANE; PALLADIUM COMPLEX; VINYL ACETATE;

EID: 56949108835     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.09.108     Document Type: Article
Times cited : (33)

References (40)
  • 35
    • 56949108812 scopus 로고    scopus 로고
    • note
    • 2 (X = Cl, Br) and benzoquinone, were ineffective.
  • 37
    • 0025953513 scopus 로고
    • The stereochemistry of 2i and 2j was assigned by NMR spectroscopy using NOE experiments and comparison with known analogues:
    • The stereochemistry of 2i and 2j was assigned by NMR spectroscopy using NOE experiments and comparison with known analogues:. Berrier C., Bonnaud B., Patoiseau J.F., and Bigg D. Tetrahedron 47 (1991) 9629-9640
    • (1991) Tetrahedron , vol.47 , pp. 9629-9640
    • Berrier, C.1    Bonnaud, B.2    Patoiseau, J.F.3    Bigg, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.