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Volumn , Issue 22, 2007, Pages 3727-3745

Synthesis of cyclic and macrocyclic ethers using metathesis reactions of alkenes and alkynes

Author keywords

Macrocycles; Medium ring compounds; Metathesis; Oxygen heterocycles; Ruthenium

Indexed keywords


EID: 34547669257     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700291     Document Type: Article
Times cited : (21)

References (57)
  • 1
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    • For recent reviews of the development and applications of ruthenium based metathesis initiators see: a R. H. Grubbs, Adv. Synth. Catal. 2007, 349, 34-40;
    • For recent reviews of the development and applications of ruthenium based metathesis initiators see: a) R. H. Grubbs, Adv. Synth. Catal. 2007, 349, 34-40;
  • 10
    • 33846665005 scopus 로고    scopus 로고
    • For recent reviews of enyne metathesis see:a
    • For recent reviews of enyne metathesis see:a) M. Mori, Adv. Synth. Catal. 2007, 349, 121-135;
    • (2007) Adv. Synth. Catal , vol.349 , pp. 121-135
    • Mori, M.1
  • 19
    • 33846689012 scopus 로고    scopus 로고
    • For a preliminary account of some of the work reported in this manuscript see
    • For a preliminary account of some of the work reported in this manuscript see: E. Groaz, D. Banti, M. North, Adv. Synth. Catal. 2007, 349, 142-146.
    • (2007) Adv. Synth. Catal , vol.349 , pp. 142-146
    • Groaz, E.1    Banti, D.2    North, M.3
  • 20
    • 0035929110 scopus 로고    scopus 로고
    • For a previous report of cyclohexene ring opening during cross metathesis see
    • For a previous report of cyclohexene ring opening during cross metathesis see: S. Randl, S. J. Connon, S. Blechert, Chem. Commun. 2001, 1796-1797.
    • (2001) Chem. Commun , pp. 1796-1797
    • Randl, S.1    Connon, S.J.2    Blechert, S.3
  • 21
    • 33846703743 scopus 로고    scopus 로고
    • For reviews of alkyne metathesis see:a
    • For reviews of alkyne metathesis see:a) W. Zhang, J. S. Moore, Adv. Synth. Catal. 2007, 349, 93-120;
    • (2007) Adv. Synth. Catal , vol.349 , pp. 93-120
    • Zhang, W.1    Moore, J.S.2
  • 26
    • 0033617426 scopus 로고    scopus 로고
    • 13C NMR spectra of compound 10 are given in the supplementary information to this paper.
    • 13C NMR spectra of compound 10 are given in the supplementary information to this paper.
  • 28
    • 0035912321 scopus 로고    scopus 로고
    • For previous reports of enyne metathesis involving ring-opening of a cyclohexene unit see: a
    • For previous reports of enyne metathesis involving ring-opening of a cyclohexene unit see: a) T. Kitamura, M. Mori, Org. Lett. 2001, 3, 1161-1163;
    • (2001) Org. Lett , vol.3 , pp. 1161-1163
    • Kitamura, T.1    Mori, M.2
  • 29
    • 3242888384 scopus 로고    scopus 로고
    • T. Kitamura, Y. Kuzuba, Y. Sato, H. Wakamatsu, R. Fujita, M. Mori, Tetrahedron 2004, 60, 7375-7389. See also ref.M.
    • b) T. Kitamura, Y. Kuzuba, Y. Sato, H. Wakamatsu, R. Fujita, M. Mori, Tetrahedron 2004, 60, 7375-7389. See also ref.M.
  • 30
    • 0001603182 scopus 로고    scopus 로고
    • For a related use of catalyst 1 to form eight-membered rings by enyne metathesis see: a
    • For a related use of catalyst 1 to form eight-membered rings by enyne metathesis see: a) M. Mori, T. Kitamura, N. Sakakibara, Y. Sato, Org. Lett. 2000, 2, 543-545;
    • (2000) Org. Lett , vol.2 , pp. 543-545
    • Mori, M.1    Kitamura, T.2    Sakakibara, N.3    Sato, Y.4
  • 38
    • 0034661914 scopus 로고    scopus 로고
    • For previous reports on the higher activity of catalyst 2 than catalyst 1 in enyne metathesis see: a R. Stragies, U. Voigtmann, S. Blechert, Tetrahedron Lett. 2000, 41, 5465-5468;
    • For previous reports on the higher activity of catalyst 2 than catalyst 1 in enyne metathesis see: a) R. Stragies, U. Voigtmann, S. Blechert, Tetrahedron Lett. 2000, 41, 5465-5468;
  • 42
    • 0033578944 scopus 로고    scopus 로고
    • Decomposition of ruthenium alkylidenes is known to be a second order process in contrast to the first order decomposition of methylidene complexes: M. Ulman, R. H. Grubbs, J. Org. Chem. 1999, 64, 7202-7207
    • Decomposition of ruthenium alkylidenes is known to be a second order process in contrast to the first order decomposition of methylidene complexes: M. Ulman, R. H. Grubbs, J. Org. Chem. 1999, 64, 7202-7207.
  • 48
    • 0035905420 scopus 로고    scopus 로고
    • For examples of the formation of eleven-membered rings in low yields see: a A. Fürstner, C. Mathes, C. W. Lehmann, Chem. Eur. J. 2001, 7, 5299-5317;
    • For examples of the formation of eleven-membered rings in low yields see: a) A. Fürstner, C. Mathes, C. W. Lehmann, Chem. Eur. J. 2001, 7, 5299-5317;
  • 53
    • 34547650181 scopus 로고    scopus 로고
    • R. R. Schrock, in Handbook of Metathesis, 1, Catalyst Development (Ed.: R. H. Grubbs), Wiley-VCH, Weinheim. Germany, 2003, pp. 173-189.
    • b) R. R. Schrock, in Handbook of Metathesis, vol. 1, Catalyst Development (Ed.: R. H. Grubbs), Wiley-VCH, Weinheim. Germany, 2003, pp. 173-189.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.