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Volumn , Issue 10, 2006, Pages 1527-1530

Enantioselective synthesis of bicyclo[4.4.1]undecane-2,7-dione via samarium(II)-mediated fragmentation of a cyclopropane precursor

Author keywords

Asymmetric synthesis; Chirality; Cyclopropane; Fragmentation; Samarium diiodide

Indexed keywords

2,3,4,6,7,8 HEXAHYDRONAPHTHALENE 1,5 DIONE; BICYCLO[4.4.1]UNDECANE 2,7 DIONE; CYCLOPROPANE; DIKETONE; KETONE DERIVATIVE; OXAZABOROLIDINE DERIVATIVE; SAMARIUM; SAMARIUM IODIDE; TRICYCLO[4.4.1.0 1,6]UNDECANE 2,7 DIONE; UNCLASSIFIED DRUG;

EID: 33745698046     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-941599     Document Type: Article
Times cited : (16)

References (32)
  • 4
    • 4644344337 scopus 로고    scopus 로고
    • 1-bridge) also occurs as a substructure in some other more complex polycyclic natural products such as ingenol. For a leading reference, see: Montalt, J.; Linker, F.; Ratel, F.; Miesch, M. J. Org. Chem. 2004, 69, 6715.
    • (2004) J. Org. Chem. , vol.69 , pp. 6715
    • Montalt, J.1    Linker, F.2    Ratel, F.3    Miesch, M.4
  • 31
    • 0001606659 scopus 로고
    • The homologous (1R,5R)-bicyclo[3.3.1]nonane-2,6-dione also displays a negative Cotton effect: (a) Berg, U.; Butkus, E. J. Chem. Res., Synop. 1993, 116.
    • (1993) J. Chem. Res., Synop. , pp. 116
    • Berg, U.1    Butkus, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.