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Volumn 8, Issue 17, 2010, Pages 4016-4025

Unexpected iron(iii) chloride-catalysed dimerisation of 1,1,3-trisubstituted-prop-2-yn-1-ols as an expedient route to highly conjugated indenes

Author keywords

[No Author keywords available]

Indexed keywords

GOOD YIELD; IRON CHLORIDES; PROPARGYLIC ALCOHOLS; ROOM TEMPERATURE;

EID: 77955487688     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c003522j     Document Type: Article
Times cited : (12)

References (106)
  • 79
    • 33846954037 scopus 로고    scopus 로고
    • Please see the Electronic Supplementary Information for details Apparent 1,3-alkyl migrations have also been proposed in other reactions, for selected examples see:
    • L. Peng X. Zhang S. Zhang J. Wang J. Org. Chem. 2007 72 1192
    • (2007) J. Org. Chem. , vol.72 , pp. 1192
    • Peng, L.1    Zhang, X.2    Zhang, S.3    Wang, J.4
  • 86
    • 37049096384 scopus 로고
    • For examples of Lewis acid-catalysed formation of propargylic cations and similar regioselectivities observed in these reactions, see ref. 4-7 and:
    • K. Takagi Y. Ogata J. Chem. Soc., Perkin Trans. 2 1977 1410
    • (1977) J. Chem. Soc., Perkin Trans. 2 , pp. 1410
    • Takagi, K.1    Ogata, Y.2
  • 90
    • 0035967754 scopus 로고    scopus 로고
    • The addition of an acetylenic moiety to a carbocation centre has also been proposed in other reactions, for selected examples see ref. 7aand
    • T. Ishikawa M. Okano T. Aikawa S. Saito J. Org. Chem. 2001 66 4635
    • (2001) J. Org. Chem. , vol.66 , pp. 4635
    • Ishikawa, T.1    Okano, M.2    Aikawa, T.3    Saito, S.4
  • 99


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.