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Volumn 7, Issue 21, 2005, Pages 4553-4556

Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate

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EID: 27144523211     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051065f     Document Type: Article
Times cited : (167)

References (41)
  • 1
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    • Yamamoto, H., Ed.; Wiley-VCH: Weinheim, Germany, Chapter 13
    • Yanagisawa, A. Lewis Acids in Organic Synthesis; Yamamoto, H., Ed.; Wiley-VCH: Weinheim, Germany, 2000; Vol. 2, Chapter 13.
    • (2000) Lewis Acids in Organic Synthesis , vol.2
    • Yanagisawa, A.1
  • 2
    • 2342512074 scopus 로고    scopus 로고
    • For selected examples on Aldol-type reactions, see: (a) Momiyama, N.; Yamamoto, H. J. Am. Chem. Soc. 2004, 126, 5360-5361.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5360-5361
    • Momiyama, N.1    Yamamoto, H.2
  • 11
    • 0037073234 scopus 로고    scopus 로고
    • For selected examples on [3 + 2] cycloaddition of azomethine ylides, see: (a) Longmire, J. M.; Wang, B.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 13400-13401.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13400-13401
    • Longmire, J.M.1    Wang, B.2    Zhang, X.3
  • 16
    • 0000419893 scopus 로고    scopus 로고
    • For epoxide rearrangement, see: Wipf, P.; Methot, J.-L. Org. Lett. 1999, 1, 1253-1255.
    • (1999) Org. Lett. , vol.1 , pp. 1253-1255
    • Wipf, P.1    Methot, J.-L.2
  • 22
    • 0037634729 scopus 로고
    • For reviews encompassing Ag(I)-alkene complexes, see: (a) Bennett, M. A. Chem. Rev. 1962, 62, 611-652.
    • (1962) Chem. Rev. , vol.62 , pp. 611-652
    • Bennett, M.A.1
  • 25
    • 0342859713 scopus 로고
    • Elsevier: Amsterdam
    • (d) Herberhold, M. In Metal-π-Complexes; Elsevier: Amsterdam, 1972; Vol. 2, pp 232-256.
    • (1972) Metal-π-Complexes , vol.2 , pp. 232-256
    • Herberhold, M.1
  • 31
  • 40
    • 27144481577 scopus 로고    scopus 로고
    • note
    • For details, see Figures S1-S13 in the Supporting Information.
  • 41
    • 0029833299 scopus 로고    scopus 로고
    • The assignment of the stereochemistry of compound 7 is based on the 2D NMR experiments (for details, see the Supporting Information). Similarly, we determine the stereochemistry of compound 10 by comparison with compound 7. And also see: Doyle, M. P.; Kalinin, A. V.; Ene, D. G. J. Am. Chem. Soc. 1996, 118, 8837-8846.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 8837-8846
    • Doyle, M.P.1    Kalinin, A.V.2    Ene, D.G.3


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