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Volumn 6, Issue 4, 2004, Pages 569-572

Synthesis of the C16-C35 Fragment of Integramycin Using Olefin Hydroesterification as a Linchpin Reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALKENE; ALLYL COMPOUND; INTEGRAMYCIN; INTEGRASE INHIBITOR; LACTONE; RUTHENIUM DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1342290260     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol036339i     Document Type: Article
Times cited : (42)

References (25)
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    • Prepared in three steps from commercialy available 3,5-dihydroxy-benzoic acid, (a) Stewart, G. M.; Fox, M. A. J. Am. Chem. Soc. 1996, 118, 4354. (b) Lupton, J. M.; Hemingway, L. R.; Samuel, I. D. W.; Burn, P. L. J. Mater. Chem. 2000, 10, 867. (c) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95.
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    • Stewart, G.M.1    Fox, M.A.2
  • 8
    • 0034039939 scopus 로고    scopus 로고
    • Prepared in three steps from commercialy available 3,5-dihydroxy-benzoic acid, (a) Stewart, G. M.; Fox, M. A. J. Am. Chem. Soc. 1996, 118, 4354. (b) Lupton, J. M.; Hemingway, L. R.; Samuel, I. D. W.; Burn, P. L. J. Mater. Chem. 2000, 10, 867. (c) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95.
    • (2000) J. Mater. Chem. , vol.10 , pp. 867
    • Lupton, J.M.1    Hemingway, L.R.2    Samuel, I.D.W.3    Burn, P.L.4
  • 9
    • 0030979224 scopus 로고    scopus 로고
    • Prepared in three steps from commercialy available 3,5-dihydroxy-benzoic acid, (a) Stewart, G. M.; Fox, M. A. J. Am. Chem. Soc. 1996, 118, 4354. (b) Lupton, J. M.; Hemingway, L. R.; Samuel, I. D. W.; Burn, P. L. J. Mater. Chem. 2000, 10, 867. (c) Orsini, F.; Pelizzoni, F.; Bellini, B.; Miglierini, G. Carbohydr. Res. 1997, 301, 95.
    • (1997) Carbohydr. Res. , vol.301 , pp. 95
    • Orsini, F.1    Pelizzoni, F.2    Bellini, B.3    Miglierini, G.4
  • 14
    • 0141451922 scopus 로고    scopus 로고
    • For examples, see: (a) Cossy, J.; Bargiggia, F.; BouzBouz, S. Org. Lett. 2003, 4, 459. (b) Louie, J.; Bielawski, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 11312. (c) Wuts, P. G.; Obrzut, M. L.; Thompson, P. A. Tetrahedron Lett. 1984, 25, 4051. (d) Wipf, P.; Reeves, J. T. Chem. Commun. 2002, 2066.
    • (2003) Org. Lett. , vol.4 , pp. 459
    • Cossy, J.1    Bargiggia, F.2    BouzBouz, S.3
  • 15
    • 0035861034 scopus 로고    scopus 로고
    • For examples, see: (a) Cossy, J.; Bargiggia, F.; BouzBouz, S. Org. Lett. 2003, 4, 459. (b) Louie, J.; Bielawski, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 11312. (c) Wuts, P. G.; Obrzut, M. L.; Thompson, P. A. Tetrahedron Lett. 1984, 25, 4051. (d) Wipf, P.; Reeves, J. T. Chem. Commun. 2002, 2066.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11312
    • Louie, J.1    Bielawski, C.W.2    Grubbs, R.H.3
  • 16
    • 0000274491 scopus 로고
    • For examples, see: (a) Cossy, J.; Bargiggia, F.; BouzBouz, S. Org. Lett. 2003, 4, 459. (b) Louie, J.; Bielawski, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 11312. (c) Wuts, P. G.; Obrzut, M. L.; Thompson, P. A. Tetrahedron Lett. 1984, 25, 4051. (d) Wipf, P.; Reeves, J. T. Chem. Commun. 2002, 2066.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 4051
    • Wuts, P.G.1    Obrzut, M.L.2    Thompson, P.A.3
  • 17
    • 0036401436 scopus 로고    scopus 로고
    • For examples, see: (a) Cossy, J.; Bargiggia, F.; BouzBouz, S. Org. Lett. 2003, 4, 459. (b) Louie, J.; Bielawski, C. W.; Grubbs, R. H. J. Am. Chem. Soc. 2001, 123, 11312. (c) Wuts, P. G.; Obrzut, M. L.; Thompson, P. A. Tetrahedron Lett. 1984, 25, 4051. (d) Wipf, P.; Reeves, J. T. Chem. Commun. 2002, 2066.
    • (2002) Chem. Commun. , pp. 2066
    • Wipf, P.1    Reeves, J.T.2


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