-
1
-
-
0037048468
-
-
For recent syntheses of tiazofurin, see:
-
For recent syntheses of tiazofurin, see:. Brown R.S., Dowden J., Moreau C., and Potter B.V.L. Tetrahedron Lett. 43 (2002) 6561
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6561
-
-
Brown, R.S.1
Dowden, J.2
Moreau, C.3
Potter, B.V.L.4
-
6
-
-
1842431902
-
-
Pankiewicz K.W., Patterson S.E., Black P.L., Jayaram H.N., Risal D., Goldstein B.M., Stuyver L.J., and Schinazi R.F. Curr. Med. Chem. 11 (2004) 887
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 887
-
-
Pankiewicz, K.W.1
Patterson, S.E.2
Black, P.L.3
Jayaram, H.N.4
Risal, D.5
Goldstein, B.M.6
Stuyver, L.J.7
Schinazi, R.F.8
-
7
-
-
0026775824
-
-
Szekeres T., Fitzer M., Pillwein K., Felzmann T., and Chiba P. Life Sci. 51 (1992) 1309
-
(1992)
Life Sci.
, vol.51
, pp. 1309
-
-
Szekeres, T.1
Fitzer, M.2
Pillwein, K.3
Felzmann, T.4
Chiba, P.5
-
8
-
-
4544366831
-
-
and references therein
-
Malek K., Boosalis M., Waraska K., Mitchell B.S., and Wright D.G. Leuk. Res. 28 (2004) 1125 and references therein
-
(2004)
Leuk. Res.
, vol.28
, pp. 1125
-
-
Malek, K.1
Boosalis, M.2
Waraska, K.3
Mitchell, B.S.4
Wright, D.G.5
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9
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26644464171
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-
For recent syntheses of tiazofurin analogues with modified sugar moieties, see:
-
For recent syntheses of tiazofurin analogues with modified sugar moieties, see:. Chun M.W., Kim M.J., Shin J.H., and Jeong L.S. Nucleosides Nucleotides Nucleic Acids 24 (2005) 975
-
(2005)
Nucleosides Nucleotides Nucleic Acids
, vol.24
, pp. 975
-
-
Chun, M.W.1
Kim, M.J.2
Shin, J.H.3
Jeong, L.S.4
-
10
-
-
8844225981
-
-
-
Nair V., and Wenzel T. ARKIVOC 14 (2004) 128. http://arkat-usa.alfahosting.net/ark/journal/2004/I14_General/1184/04-1184B.pdf
-
(2004)
ARKIVOC
, vol.14
, pp. 128
-
-
Nair, V.1
Wenzel, T.2
-
12
-
-
0141648324
-
-
Cappellacci L., Barboni G., Franchetti P., Martini C., Jayaram H.N., and Grifantini M. Nucleosides Nucleotides Nucleic Acids 22 (2003) 869
-
(2003)
Nucleosides Nucleotides Nucleic Acids
, vol.22
, pp. 869
-
-
Cappellacci, L.1
Barboni, G.2
Franchetti, P.3
Martini, C.4
Jayaram, H.N.5
Grifantini, M.6
-
13
-
-
0032536064
-
-
Zhang H.Y., Yu H.W., Ma L.T., Min J.M., and Zhang L.H. Tetrahedron: Asymmetry 9 (1998) 141
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 141
-
-
Zhang, H.Y.1
Yu, H.W.2
Ma, L.T.3
Min, J.M.4
Zhang, L.H.5
-
14
-
-
0041831043
-
-
Popsavin M., Torović Lj., Kojić V., Bogdanović G., Spaić S., and Popsavin V. Bioorg. Med. Chem. Lett. 13 (2003) 3167
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3167
-
-
Popsavin, M.1
Torović, Lj.2
Kojić, V.3
Bogdanović, G.4
Spaić, S.5
Popsavin, V.6
-
15
-
-
4444353861
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-
Popsavin M., Torović Lj., Kojić V., Bogdanović G., and Popsavin V. Tetrahedron. Lett. 45 (2004) 7125
-
(2004)
Tetrahedron. Lett.
, vol.45
, pp. 7125
-
-
Popsavin, M.1
Torović, Lj.2
Kojić, V.3
Bogdanović, G.4
Popsavin, V.5
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16
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0028764311
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Popsavin M., Popsavin V., Vukojević N., Csanádi J., and Miljković D. Carbohydr. Res. 260 (1994) 145
-
(1994)
Carbohydr. Res.
, vol.260
, pp. 145
-
-
Popsavin, M.1
Popsavin, V.2
Vukojević, N.3
Csanádi, J.4
Miljković, D.5
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17
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33645890805
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note
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++H).
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-
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18
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33645851894
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note
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++H).
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19
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33645853117
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note
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After shorter reaction time, the main reaction product was accompanied with the thiocarboxamide bearing an unchanged azido group at C-2. This proves that addition of hydrogen sulfide to the nitrile group precedes reduction of the azido function.
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21
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33645880371
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note
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5S: C, 50.40; H, 6.49, N, 11.76; S, 8.97. Found: C, 50.12; H, 6.21, N, 11.96; S, 8.66.
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-
-
-
22
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33645892836
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note
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5S: C, 57.12; H, 7.99, N, 9.52; S, 7.26. Found: C, 56.92; H, 7.77, N, 9.86; S, 6.90.
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-
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23
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0023792919
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Scudiero D.A., Shoemaker R.H., Paull K.D., Monks A., Tierney S., Nofziger T.H., Currens M.J., Seniff D., and Boyd M.R. Cancer. Res. 48 (1988) 4827
-
(1988)
Cancer. Res.
, vol.48
, pp. 4827
-
-
Scudiero, D.A.1
Shoemaker, R.H.2
Paull, K.D.3
Monks, A.4
Tierney, S.5
Nofziger, T.H.6
Currens, M.J.7
Seniff, D.8
Boyd, M.R.9
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