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Volumn 9, Issue 22, 2011, Pages 7904-7912

Decarboxylative Claisen rearrangement reactions: Synthesis and reactivity of alkylidene-substituted indolines

Author keywords

[No Author keywords available]

Indexed keywords

ACETATE DERIVATIVES; CLAISEN REARRANGEMENT; MICROWAVE-ASSISTED;

EID: 80055018081     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06212c     Document Type: Article
Times cited : (18)

References (43)
  • 11
    • 4344610661 scopus 로고    scopus 로고
    • For a review of catalysis of the Claisen rearrangement, see
    • A. M. Castro Chem. Rev. 2004 104 2939
    • (2004) Chem. Rev. , vol.104 , pp. 2939
    • Castro, A.M.1
  • 13
    • 29044439096 scopus 로고    scopus 로고
    • For other transiently de-aromatising sigmatropic rearrangement reactions of furans, which gave aromatic products, see
    • D. Craig N. P. King J. T. Kley D. M. Mountford Synthesis 2005 3279
    • (2005) Synthesis , pp. 3279
    • Craig, D.1    King, N.P.2    Kley, J.T.3    Mountford, D.M.4
  • 26
    • 70349111492 scopus 로고    scopus 로고
    • For other de-aromatising sigmatropic rearrangement reactions of heteroaromatic substrates, which gave isolable, non-aromatic products, see
    • Y.-J. Li Y.-K. Chang G.-M. Ho H.-M. Huang Org. Lett. 2009 11 4224
    • (2009) Org. Lett. , vol.11 , pp. 4224
    • Li, Y.-J.1    Chang, Y.-K.2    Ho, G.-M.3    Huang, H.-M.4
  • 35
    • 80055012089 scopus 로고    scopus 로고
    • Solvents which we have found to be effective in other dCr reactions, such as DMF and MeCN performed poorly in these transformations. See:, PhD thesis, Imperial College, 2009
    • Solvents which we have found to be effective in other dCr reactions, such as DMF and MeCN performed poorly in these transformations. See: S. J. Gore, PhD thesis, Imperial College, 2009
    • Gore, S.J.1
  • 37
    • 1642565858 scopus 로고    scopus 로고
    • max = 58°], 295 parameters. CCDC It is not clear why 1,2-addition of TsH is not observed across the C3-vinyl group in the second of the two dienes formed during conversion of 2h into 3. We thank a referee for raising this point For examples, see
    • J. Siu I. R. Baxendale S. V. Ley Org. Biomol. Chem. 2004 2 160
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 160
    • Siu, J.1    Baxendale, I.R.2    Ley, S.V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.