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Volumn 44, Issue 51, 2003, Pages 9177-9180

A new route to acyclic nucleosides via palladium-mediated allylic alkylation and cross-metathesis

Author keywords

Acyclonucleosides; Cross metathesis; Palladium mediated allylic alkylation

Indexed keywords

ALLYL COMPOUND; NUCLEOSIDE DERIVATIVE; PALLADIUM; RUTHENIUM;

EID: 0344413521     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.10.029     Document Type: Article
Times cited : (28)

References (39)
  • 4
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    • Kluwer Academic Publishers: Dordrecht; Chapters 1 and 2
    • For reviews on acyclic nucleosides, see: (a) Agrofoglio, L. A.; Challand, S. R. Acyclic, Carbocyclic and L-Nucleosides; Kluwer Academic Publishers: Dordrecht, 1998; Chapters 1 and 2; (b) Chu, C. K.; Cutler, S. J. J. Heterocyclic Chem. 1986, 23, 289-319; (c) De Clerq, E.; Holy, A.; Rosenberg, I. ; Sakuma, T.; Balzarini, J.; Maudgal, P. C. Nature 1986, 323, 464-467; (d) Naesens, L.; Snoeck, R.; Andrei, G.; Balzarini, J.; Neyts, J.; De Clercq, E. Antiviral Chem. Chemother. 1997, 8, 1-23.
    • (1998) Acyclic, Carbocyclic and L-Nucleosides
    • Agrofoglio, L.A.1    Challand, S.R.2
  • 5
    • 0022532716 scopus 로고
    • For reviews on acyclic nucleosides, see: (a) Agrofoglio, L. A.; Challand, S. R. Acyclic, Carbocyclic and L-Nucleosides; Kluwer Academic Publishers: Dordrecht, 1998; Chapters 1 and 2; (b) Chu, C. K.; Cutler, S. J. J. Heterocyclic Chem. 1986, 23, 289-319; (c) De Clerq, E.; Holy, A.; Rosenberg, I. ; Sakuma, T.; Balzarini, J.; Maudgal, P. C. Nature 1986, 323, 464-467; (d) Naesens, L.; Snoeck, R.; Andrei, G.; Balzarini, J.; Neyts, J.; De Clercq, E. Antiviral Chem. Chemother. 1997, 8, 1-23.
    • (1986) J. Heterocyclic Chem. , vol.23 , pp. 289-319
    • Chu, C.K.1    Cutler, S.J.2
  • 6
    • 0022450584 scopus 로고
    • For reviews on acyclic nucleosides, see: (a) Agrofoglio, L. A.; Challand, S. R. Acyclic, Carbocyclic and L-Nucleosides; Kluwer Academic Publishers: Dordrecht, 1998; Chapters 1 and 2; (b) Chu, C. K.; Cutler, S. J. J. Heterocyclic Chem. 1986, 23, 289-319; (c) De Clerq, E.; Holy, A.; Rosenberg, I. ; Sakuma, T.; Balzarini, J.; Maudgal, P. C. Nature 1986, 323, 464-467; (d) Naesens, L.; Snoeck, R.; Andrei, G.; Balzarini, J.; Neyts, J.; De Clercq, E. Antiviral Chem. Chemother. 1997, 8, 1-23.
    • (1986) Nature , vol.323 , pp. 464-467
    • De Clerq, E.1    Holy, A.2    Rosenberg, I.3    Sakuma, T.4    Balzarini, J.5    Maudgal, P.C.6
  • 7
    • 0031036704 scopus 로고    scopus 로고
    • For reviews on acyclic nucleosides, see: (a) Agrofoglio, L. A.; Challand, S. R. Acyclic, Carbocyclic and L-Nucleosides; Kluwer Academic Publishers: Dordrecht, 1998; Chapters 1 and 2; (b) Chu, C. K.; Cutler, S. J. J. Heterocyclic Chem. 1986, 23, 289-319; (c) De Clerq, E.; Holy, A.; Rosenberg, I. ; Sakuma, T.; Balzarini, J.; Maudgal, P. C. Nature 1986, 323, 464-467; (d) Naesens, L.; Snoeck, R.; Andrei, G.; Balzarini, J.; Neyts, J.; De Clercq, E. Antiviral Chem. Chemother. 1997, 8, 1-23.
    • (1997) Antiviral Chem. Chemother. , vol.8 , pp. 1-23
    • Naesens, L.1    Snoeck, R.2    Andrei, G.3    Balzarini, J.4    Neyts, J.5    De Clercq, E.6
  • 8
    • 0037944068 scopus 로고    scopus 로고
    • For a recent review on palladium-assisted routes to nucleosides, see:
    • For a recent review on palladium-assisted routes to nucleosides, see: Agrofoglio L.A., Gillaizeau I., Saito Y. Chem. Rev. 103:2003;1875-1916.
    • (2003) Chem. Rev. , vol.103 , pp. 1875-1916
    • Agrofoglio, L.A.1    Gillaizeau, I.2    Saito, Y.3
  • 9
    • 0000755941 scopus 로고    scopus 로고
    • For reviews on metathesis, see: (a) Schuster, M.; Blechert, S. Angew. Chem., Int. Ed. Engl. 1997, 36, 2037-2056; (b) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012-3043.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 2037-2056
    • Schuster, M.1    Blechert, S.2
  • 10
    • 0001399412 scopus 로고    scopus 로고
    • For reviews on metathesis, see: (a) Schuster, M.; Blechert, S. Angew. Chem., Int. Ed. Engl. 1997, 36, 2037-2056; (b) Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012-3043.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012-3043
    • Fürstner, A.1
  • 17
    • 0344181940 scopus 로고    scopus 로고
    • note
    • max 284 nm.
  • 34
    • 0345044469 scopus 로고    scopus 로고
    • note
    • max 270 nm.
  • 37
    • 0345475853 scopus 로고    scopus 로고
    • note
    • max 265 nm.
  • 38
    • 0035208486 scopus 로고    scopus 로고
    • For a synthetic procedure describing allyl acetate 12 involving several steps. See: (a) Sugisaki, C. H.; Ruland, Y.; Le Clezio, I.; Baltas, M. Synlett 2001, 1905-1908; (b) Takano, S.; Iwabuchi, Y.; Ogasawara, K. Synlett 1991, 548-550.
    • (2001) Synlett , pp. 1905-1908
    • Sugisaki, C.H.1    Ruland, Y.2    Le Clezio, I.3    Baltas, M.4
  • 39
    • 84987511469 scopus 로고
    • For a synthetic procedure describing allyl acetate 12 involving several steps. See: (a) Sugisaki, C. H.; Ruland, Y.; Le Clezio, I.; Baltas, M. Synlett 2001, 1905-1908; (b) Takano, S.; Iwabuchi, Y.; Ogasawara, K. Synlett 1991, 548-550.
    • (1991) Synlett , pp. 548-550
    • Takano, S.1    Iwabuchi, Y.2    Ogasawara, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.