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Volumn 11, Issue 8, 2009, Pages 1673-1675

Polyene cyclization promoted by the cross-conjugated α-carbalkoxy cyclohexenone system. An unusual 1,2-hydride shift under lewis acid catalysis

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM CHLORIDE; ALUMINUM DERIVATIVE; CHLORIDE; CYCLOHEXANONE DERIVATIVE; POLYCYCLIC HYDROCARBON; POLYENE; STANNOUS CHLORIDE; TIN DERIVATIVE;

EID: 65249085747     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol802878t     Document Type: Article
Times cited : (11)

References (29)
  • 8
    • 0000013070 scopus 로고    scopus 로고
    • Marshall, J. M.; Wuts, P. G. A. J.Org. Chem. 1977. 42, 1794.
    • (c) Marshall, J. M.; Wuts, P. G. A. J.Org. Chem. 1977. 42, 1794.
  • 19
    • 65249157621 scopus 로고    scopus 로고
    • CCDC 261323 (7a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc. cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
    • CCDC 261323 (7a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc. cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
  • 20
    • 65249093449 scopus 로고    scopus 로고
    • All the 1,2-hydride shifts represented in the paper are presumably reversible
    • All the 1,2-hydride shifts represented in the paper are presumably reversible.
  • 21
    • 65249184779 scopus 로고    scopus 로고
    • CCDC 261322 (8a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc. cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
    • CCDC 261322 (8a) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc. cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
  • 22
    • 65249143693 scopus 로고    scopus 로고
    • Although 8b was obtained as a single diastereomer in an enol form as indicated by its 1H NMR spectrum, to rule out any undesired signals from other potential isomers, the labile stereogenic center linked to the carbonyl was destroyed by acetylation to give acetate 9 prior to performing NOE experiments
    • 1H NMR spectrum, to rule out any undesired signals from other potential isomers, the labile stereogenic center linked to the carbonyl was destroyed by acetylation to give acetate 9 prior to performing NOE experiments.
  • 23
    • 65249147523 scopus 로고    scopus 로고
    • CCDC 701542 (10) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
    • CCDC 701542 (10) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html or deposite@ccdc.cam.ac.uk.
  • 26
    • 35548987589 scopus 로고    scopus 로고
    • Robins, M. J.; Nowak, 1.; Wnuk, S. F.; Hansske, F.; Madej, D. J.Org. Chem. 2007, 72, 8216.
    • (c) Robins, M. J.; Nowak, 1.; Wnuk, S. F.; Hansske, F.; Madej, D. J.Org. Chem. 2007, 72, 8216.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.