메뉴 건너뛰기




Volumn 125, Issue 32, 2003, Pages 9582-9583

Enyne metathesis for the formation of macrocyclic 1,3-dienes

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE; MACROCYCLIC COMPOUND;

EID: 0042626460     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja036374k     Document Type: Article
Times cited : (69)

References (31)
  • 1
    • 0032580376 scopus 로고    scopus 로고
    • For reviews of olefin metathesis, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413. (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371. (c) Furstner, A. Angew. Chem., Int. Ed. 2000, 39, 3013. (d) Connon, S. J.; Blechert, S. Angew. Chem., Int. Ed. 2003, 42, 1900.
    • (1998) Tetrahedron , vol.54 , pp. 4413
    • Grubbs, R.H.1    Chang, S.2
  • 2
    • 28244440935 scopus 로고    scopus 로고
    • For reviews of olefin metathesis, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413. (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371. (c) Furstner, A. Angew. Chem., Int. Ed. 2000, 39, 3013. (d) Connon, S. J.; Blechert, S. Angew. Chem., Int. Ed. 2003, 42, 1900.
    • (1998) J. Chem. Soc., Perkin Trans. 1 , pp. 371
    • Armstrong, S.K.1
  • 3
    • 0344006321 scopus 로고    scopus 로고
    • For reviews of olefin metathesis, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413. (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371. (c) Furstner, A. Angew. Chem., Int. Ed. 2000, 39, 3013. (d) Connon, S. J.; Blechert, S. Angew. Chem., Int. Ed. 2003, 42, 1900.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3013
    • Furstner, A.1
  • 4
    • 0038215596 scopus 로고    scopus 로고
    • For reviews of olefin metathesis, see: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413. (b) Armstrong, S. K. J. Chem. Soc., Perkin Trans. 1 1998, 371. (c) Furstner, A. Angew. Chem., Int. Ed. 2000, 39, 3013. (d) Connon, S. J.; Blechert, S. Angew. Chem., Int. Ed. 2003, 42, 1900.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 1900
    • Connon, S.J.1    Blechert, S.2
  • 12
    • 33845379363 scopus 로고
    • Katz, T. J.; Sivavec, T. M. J. Am. Chem. Soc. 1985, 107, 737. For the first enyne metathesis with Grubbs catalyst, see: (b) Kinoshita, A.; Mori, M. Synlett 1994, 1020. For reviews, see: (c) Poulsen, C. S.; Madsen, R. Synthesis 2003, 1. (d) Mori, M. Top. Organomet. Chem. 1998. 1, 133.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 737
    • Katz, T.J.1    Sivavec, T.M.2
  • 13
    • 85064679737 scopus 로고
    • Katz, T. J.; Sivavec, T. M. J. Am. Chem. Soc. 1985, 107, 737. For the first enyne metathesis with Grubbs catalyst, see: (b) Kinoshita, A.; Mori, M. Synlett 1994, 1020. For reviews, see: (c) Poulsen, C. S.; Madsen, R. Synthesis 2003, 1. (d) Mori, M. Top. Organomet. Chem. 1998. 1, 133.
    • (1994) Synlett , pp. 1020
    • Kinoshita, A.1    Mori, M.2
  • 14
    • 0037244612 scopus 로고    scopus 로고
    • Katz, T. J.; Sivavec, T. M. J. Am. Chem. Soc. 1985, 107, 737. For the first enyne metathesis with Grubbs catalyst, see: (b) Kinoshita, A.; Mori, M. Synlett 1994, 1020. For reviews, see: (c) Poulsen, C. S.; Madsen, R. Synthesis 2003, 1. (d) Mori, M. Top. Organomet. Chem. 1998. 1, 133.
    • (2003) Synthesis , pp. 1
    • Poulsen, C.S.1    Madsen, R.2
  • 15
    • 0000449988 scopus 로고    scopus 로고
    • Katz, T. J.; Sivavec, T. M. J. Am. Chem. Soc. 1985, 107, 737. For the first enyne metathesis with Grubbs catalyst, see: (b) Kinoshita, A.; Mori, M. Synlett 1994, 1020. For reviews, see: (c) Poulsen, C. S.; Madsen, R. Synthesis 2003, 1. (d) Mori, M. Top. Organomet. Chem. 1998. 1, 133.
    • (1998) Top. Organomet. Chem. , vol.1 , pp. 133
    • Mori, M.1
  • 23
    • 0042891588 scopus 로고    scopus 로고
    • Dimethyl ester of 5 is available from Aldrich (25 g/$65) and its monohydrolysis, see: Maycock, C. D.; Venture, M. R. Org. Lett. 2002, 4, 2035.
    • (2002) Org. Lett. , vol.4 , pp. 2035
    • Maycock, C.D.1    Venture, M.R.2
  • 25
    • 0000340818 scopus 로고    scopus 로고
    • Six-membered ring endo-product was observed with the 1, l-disubstituted ene moiety of enyne substrates, see: (a) Kitamura, T.; Sato, Y.; Mori, M. Adv. Synth. Catal. 2002, 344, 678. (b) Dolhem, F.; Lièvre C.; Demailly, G. Eur. J. Org. Chem. 2003, 2336.
    • (2002) Adv. Synth. Catal. , vol.344 , pp. 678
    • Kitamura, T.1    Sato, Y.2    Mori, M.3
  • 26
    • 0038391513 scopus 로고    scopus 로고
    • Six-membered ring endo-product was observed with the 1, l-disubstituted ene moiety of enyne substrates, see: (a) Kitamura, T.; Sato, Y.; Mori, M. Adv. Synth. Catal. 2002, 344, 678. (b) Dolhem, F.; Lièvre C.; Demailly, G. Eur. J. Org. Chem. 2003, 2336.
    • (2003) Eur. J. Org. Chem. , pp. 2336
    • Dolhem, F.1    Lièvre, C.2    Demailly, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.