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Schaeffer H.J., Beauchamp L., De Miranda P., Elion G., Bauer D.J., Collins P. Nature. 272:1978;583-585.
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0003814964
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Kluwer Academic Publishers: Dordrecht; Chapters 1 and 2
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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.
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Acyclic, Carbocyclic and L-Nucleosides
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Agrofoglio, L.A.1
Challand, S.R.2
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5
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0022532716
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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.
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Chu, C.K.1
Cutler, S.J.2
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6
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0022450584
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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.
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De Clerq, E.1
Holy, A.2
Rosenberg, I.3
Sakuma, T.4
Balzarini, J.5
Maudgal, P.C.6
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7
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0031036704
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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.
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Naesens, L.1
Snoeck, R.2
Andrei, G.3
Balzarini, J.4
Neyts, J.5
De Clercq, E.6
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8
-
-
0037944068
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For a recent review on palladium-assisted routes to nucleosides, see:
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For a recent review on palladium-assisted routes to nucleosides, see: Agrofoglio L.A., Gillaizeau I., Saito Y. Chem. Rev. 103:2003;1875-1916.
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Agrofoglio, L.A.1
Gillaizeau, I.2
Saito, Y.3
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9
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-
0000755941
-
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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.
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Schuster, M.1
Blechert, S.2
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10
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0001399412
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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.
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Fürstner, A.1
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11
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0034705359
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Freer R., Geen G.R., Ramsay T.W., Share A.C., Slater G.R., Smith N.M. Tetrahedron. 56:2000;4589-4595.
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Tetrahedron
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Freer, R.1
Geen, G.R.2
Ramsay, T.W.3
Share, A.C.4
Slater, G.R.5
Smith, N.M.6
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13
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-
0029013539
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Lee M.-G., Lee D., Zhao Y., Newton M.G., Chun M.W., Chu C.K. Tetrahedron Lett. 36:1995;3499-3502.
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Lee, M.-G.1
Lee, D.2
Zhao, Y.3
Newton, M.G.4
Chun, M.W.5
Chu, C.K.6
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16
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0030575356
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Goux C., Sigismondi S., Sinou D., Pérez M., Moreno-Manas M., Peixats R., Villaroya M. Tetrahedron. 52:1996;9521-9534.
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Goux, C.1
Sigismondi, S.2
Sinou, D.3
Pérez, M.4
Moreno-Manas, M.5
Peixats, R.6
Villaroya, M.7
-
17
-
-
0344181940
-
-
note
-
max 284 nm.
-
-
-
-
21
-
-
0000896091
-
-
Gundersen L.-L., Benneche T., Rise F., Gogoll A., Undheim K. Acta Chem. Scand. 46:1992;761-771.
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Acta Chem. Scand.
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Gundersen, L.-L.1
Benneche, T.2
Rise, F.3
Gogoll, A.4
Undheim, K.5
-
24
-
-
0037325055
-
-
Gillaizeau I., Lagoja I.M., Nolan S.P., Aucagne V., Rozenski J., Herdewijn P., Agrofoglio L.A. Eur. J. Org. Chem. 4:2003;666-671.
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Eur. J. Org. Chem.
, vol.4
, pp. 666-671
-
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Gillaizeau, I.1
Lagoja, I.M.2
Nolan, S.P.3
Aucagne, V.4
Rozenski, J.5
Herdewijn, P.6
Agrofoglio, L.A.7
-
26
-
-
0035929402
-
-
Choi W.J., Park J.G., Yoo S.J., Kim H.O., Moon H.R., Chun M.W., Jung Y.H., Jeong L.S. J. Org. Chem. 66:2001;6490-6494.
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J. Org. Chem.
, vol.66
, pp. 6490-6494
-
-
Choi, W.J.1
Park, J.G.2
Yoo, S.J.3
Kim, H.O.4
Moon, H.R.5
Chun, M.W.6
Jung, Y.H.7
Jeong, L.S.8
-
34
-
-
0345044469
-
-
note
-
max 270 nm.
-
-
-
-
36
-
-
0035929390
-
-
Felpin F.-X., Girard S., Vo-Thanh G., Robins R.J., Villieras J., Lebreton J. J. Org. Chem. 66:2001;6305-6312.
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J. Org. Chem.
, vol.66
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-
-
Felpin, F.-X.1
Girard, S.2
Vo-Thanh, G.3
Robins, R.J.4
Villieras, J.5
Lebreton, J.6
-
37
-
-
0345475853
-
-
note
-
max 265 nm.
-
-
-
-
38
-
-
0035208486
-
-
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.
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(2001)
Synlett
, pp. 1905-1908
-
-
Sugisaki, C.H.1
Ruland, Y.2
Le Clezio, I.3
Baltas, M.4
-
39
-
-
84987511469
-
-
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
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