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Volumn 9, Issue 23, 2007, Pages 4821-4824

Gold-catalyzed hydroarylation of allenes: A highly regioselective carbon-carbon bond formation producing six-membered rings

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE; ALLENE; CARBON; GOLD; HETEROCYCLIC COMPOUND; HYDROGEN; UNCLASSIFIED DRUG;

EID: 36348979383     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702179n     Document Type: Article
Times cited : (122)

References (57)
  • 5
    • 24944520019 scopus 로고    scopus 로고
    • Krause, N, Hashmi, A. S. K, Eds, Wiley-VCH: Weinheim, Germany
    • (e) Hashmi, A. S. K. In Modern Allene Chemistry; Krause, N., Hashmi, A. S. K., Eds.; Wiley-VCH: Weinheim, Germany, 2004; Vol. 2, pp 877-923.
    • (2004) Modern Allene Chemistry , vol.2 , pp. 877-923
    • Hashmi, A.S.K.1
  • 13
    • 0037881987 scopus 로고
    • For related electrocyclization, see: a
    • For related electrocyclization, see: (a) Turnbull, P.; Moore, H. W. J. Org. Chem. 1995, 60, 3274.
    • (1995) J. Org. Chem , vol.60 , pp. 3274
    • Turnbull, P.1    Moore, H.W.2
  • 23
    • 33947578482 scopus 로고    scopus 로고
    • For recent reviews, see: a
    • For recent reviews, see: (a) Gorin, D. J.; Toste, F. D. Nature 2007, 446, 395.
    • (2007) Nature , vol.446 , pp. 395
    • Gorin, D.J.1    Toste, F.D.2
  • 28
    • 23044485049 scopus 로고    scopus 로고
    • For the reaction with oxygen nucleophiles, see: a
    • For the reaction with oxygen nucleophiles, see: (a) Sromek, A. W.; Rubina, M.; Gevorgyan, V. J. Am. Chem. Soc. 2005, 127, 10500.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 10500
    • Sromek, A.W.1    Rubina, M.2    Gevorgyan, V.3
  • 33
    • 8744284583 scopus 로고    scopus 로고
    • For the reaction with nitrogen nucleophiles, see: a
    • For the reaction with nitrogen nucleophiles, see: (a) Morita, N.; Krause, N. Org. Lett. 2004, 6, 4121.
    • (2004) Org. Lett , vol.6 , pp. 4121
    • Morita, N.1    Krause, N.2
  • 35
    • 33847664670 scopus 로고    scopus 로고
    • LaLonde, R. L.; Sherry, B. D.; Kang, E. J.; Toste, F. D. J. Am. Chem. Soc. 2007, 129, 2452. See also ref 11a.
    • (c) LaLonde, R. L.; Sherry, B. D.; Kang, E. J.; Toste, F. D. J. Am. Chem. Soc. 2007, 129, 2452. See also ref 11a.
  • 36
    • 33745652988 scopus 로고    scopus 로고
    • For the reaction with sulfur nucleophiles, see
    • For the reaction with sulfur nucleophiles, see: Morita, N.; Krause, N. Angew. Chem., Int. Ed. 2006, 45, 1897.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 1897
    • Morita, N.1    Krause, N.2
  • 41
    • 0141615958 scopus 로고    scopus 로고
    • For hydroarylation of other related substrates, see: a
    • For hydroarylation of other related substrates, see: (a) Reetz, M. T.; Sommer, K. Eur. J. Org. Chem. 2003, 3485.
    • (2003) Eur. J. Org. Chem , pp. 3485
    • Reetz, M.T.1    Sommer, K.2
  • 53
    • 36348995001 scopus 로고    scopus 로고
    • Unfortunately, synthesis of internal allenes by this approach was difficult
    • Unfortunately, synthesis of internal allenes by this approach was difficult.
  • 54
    • 18244399612 scopus 로고    scopus 로고
    • Complexes 5 and 6 were prepared according to Lopez, S.; Nieto-Oberhuber, C.; Echavarren, A. M. J. Am. Chem. Soc. 2005, 127, 6178.
    • Complexes 5 and 6 were prepared according to Lopez, S.; Nieto-Oberhuber, C.; Echavarren, A. M. J. Am. Chem. Soc. 2005, 127, 6178.
  • 55
    • 36348966075 scopus 로고    scopus 로고
    • The reaction did not proceed in AcOH without using the gold catalyst
    • The reaction did not proceed in AcOH without using the gold catalyst.
  • 56
    • 36349003706 scopus 로고    scopus 로고
    • Such reactions with Hg(II) reagent have already been reported; see ref 3. For the reactions of activated allenes, see refs 2 and 4b
    • Such reactions with Hg(II) reagent have already been reported; see ref 3. For the reactions of activated allenes, see refs 2 and 4b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.