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Volumn 688, Issue 1-2, 2003, Pages 36-48

Further studies on Ni(0)-catalyzed cyclization of a branched 1,3-diene and tethered aldehyde via oxa-nickelacycle intermediate

Author keywords

Aldehyde; Diene; Metallacycle; Nickel; Nickelacycle; Transmetalation

Indexed keywords

ALDEHYDE; ALKADIENE; CARBONYL DERIVATIVE; METAL COMPLEX; NICKEL; ORGANOMETALLIC COMPOUND; OXIDE; REAGENT;

EID: 0242571852     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2003.08.027     Document Type: Article
Times cited : (17)

References (48)
  • 1
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    • For [4+4] cycloadditions, see
    • For [4+4] cycloadditions, see: P.A. Wender, M.J. Tebbe, Synthesis (1991) 1089.
    • (1991) Synthesis , pp. 1089
    • Wender, P.A.1    Tebbe, M.J.2
  • 6
    • 0032510192 scopus 로고    scopus 로고
    • For [4+4] cycloadditions, see
    • Wender P.A. Smith T.E. Tetrahedron 54 1998 1255 For [4+4] cycloadditions, see
    • (1998) Tetrahedron , vol.54 , pp. 1255
    • Wender, P.A.1    Smith, T.E.2
  • 11
    • 85022473307 scopus 로고
    • For other cyclizations related to 1,3-dienes, see
    • For other cyclizations related to 1,3-dienes, see: K. Tamao, K. Kobayashi, Y. Ito, Synlett (1992) 539.
    • (1992) Synlett , pp. 539
    • Tamao, K.1    Kobayashi, K.2    Ito, Y.3
  • 16
    • 37049131134 scopus 로고
    • For intermolecular coupling reactions of 1,3-dienes and carbonyl compounds, see
    • For intermolecular coupling reactions of 1,3-dienes and carbonyl compounds, see: R. Baker, A.H. Cook, M.J. Crimmin, J. Chem. Soc. Chem. Commun. (1975) 727.
    • (1975) J. Chem. Soc. Chem. Commun. , pp. 727
    • Baker, R.1    Cook, A.H.2    Crimmin, M.J.3
  • 37
    • 0242670961 scopus 로고    scopus 로고
    • For spectral data of all new compounds and details for determination of the stereochemistry, see Supporting Information
    • For spectral data of all new compounds and details for determination of the stereochemistry, see Supporting Information.
  • 38
    • 0242670962 scopus 로고    scopus 로고
    • The stereochemistry of 13a or 14a was determined by its NOESY spectrum
    • The stereochemistry of 13a or 14a was determined by its NOESY spectrum.
  • 39
    • 0242502538 scopus 로고    scopus 로고
    • The stereochemistry of 23a could not be determined due to its lability
    • The stereochemistry of 23a could not be determined due to its lability.
  • 40
    • 0035809288 scopus 로고    scopus 로고
    • 2 in the presence of tetramethylethylenediamine (tmeda) have been isolated and characterized by X-ray analysis, see
    • 2 in the presence of tetramethylethylenediamine (tmeda) have been isolated and characterized by X-ray analysis, see: Amarasinghe K.K.D. Chowdhury S.K. Heeg M.J. Montgomery J. Organometallics 20 2001 370
    • (2001) Organometallics , vol.20 , pp. 370
    • Amarasinghe, K.K.D.1    Chowdhury, S.K.2    Heeg, M.J.3    Montgomery, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.