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Volumn 2, Issue 22, 2000, Pages 3477-3480

A novel synthesis of biaryl-containing macrocycles by a domino Miyaura arylboronate formation: Intramolecular Suzuki reaction

Author keywords

[No Author keywords available]

Indexed keywords

BORON DERIVATIVE; HETEROCYCLIC COMPOUND;

EID: 0034597521     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006520g     Document Type: Article
Times cited : (100)

References (52)
  • 1
    • 0031695495 scopus 로고    scopus 로고
    • (a) Shu, Y. Z. J. Nat. Prod. 1998, 61, 1053-1071.
    • (1998) J. Nat. Prod. , vol.61 , pp. 1053-1071
    • Shu, Y.Z.1
  • 23
    • 1542527790 scopus 로고    scopus 로고
    • Zhu, J. Synlett 1997, 133-134.
    • (1997) Synlett , pp. 133-134
    • Zhu, J.1
  • 34
    • 0025008669 scopus 로고
    • 3 has been used to promote the formation of six-membered rings, see: Kelly, T. R.; Li, Q.; Bhushan, V. Tetrahedron Lett. 1990, 31, 161-164. For earlier examples of ditin-mediated intermolecular cross-coupling, see: Yokoyama, Y.; Ito, S.; Takahashi, Y.; Murakami, Y. Tetrahedron Lett. 1985, 26, 6457-6460.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 161-164
    • Kelly, T.R.1    Li, Q.2    Bhushan, V.3
  • 35
    • 0000158372 scopus 로고
    • 3 has been used to promote the formation of six-membered rings, see: Kelly, T. R.; Li, Q.; Bhushan, V. Tetrahedron Lett. 1990, 31, 161-164. For earlier examples of ditin-mediated intermolecular cross-coupling, see: Yokoyama, Y.; Ito, S.; Takahashi, Y.; Murakami, Y. Tetrahedron Lett. 1985, 26, 6457-6460.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 6457-6460
    • Yokoyama, Y.1    Ito, S.2    Takahashi, Y.3    Murakami, Y.4
  • 36
    • 0033523812 scopus 로고    scopus 로고
    • Intramolecular Suzuki coupling, see: Elder, A. M.; Rich, D. H. Org. Lett. 1999, 1, 1443-1446.
    • (1999) Org. Lett. , vol.1 , pp. 1443-1446
    • Elder, A.M.1    Rich, D.H.2
  • 38
    • 0025826372 scopus 로고
    • (a) Schmidt, U.; Meyer, R.; Leitenberger, V.; Lieberknecht, A.; Griesser, H. J. Chem. Soc., Chem. Commun. 1991, 275-277. Carlström, A. S.; Frejd, T. J. Chem. Soc., Chem. Commun. 1991, 1216-1217.
    • (1991) J. Chem. Soc., Chem. Commun. , pp. 1216-1217
    • Carlström, A.S.1    Frejd, T.2
  • 43
    • 0041374980 scopus 로고    scopus 로고
    • We were unable to isolate dimer or oligomers of 11 under all these conditions. Longer reaction time (24 h) under our optimized conditions failed to improve the yield of cyclic compound
    • We were unable to isolate dimer or oligomers of 11 under all these conditions. Longer reaction time (24 h) under our optimized conditions failed to improve the yield of cyclic compound.
  • 50
    • 0042877976 scopus 로고    scopus 로고
    • DEA Dissertation, Université Paris-Sud, June These reactions have been performed in the absence of diboron ester 13.
    • Moreau-Archier, N. DEA Dissertation, Université Paris-Sud, June 1999. These reactions have been performed in the absence of diboron ester 13.
    • (1999)
    • Moreau-Archier, N.1
  • 52
    • 0042877974 scopus 로고    scopus 로고
    • note
    • +.


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