-
1
-
-
8944236567
-
-
Montreal, Canada, June 4-9, paper no. T.C.O.1
-
Belleau, B.; Dixit, D.; Nguyen-Ga, N.; Kraus, J.-L. International Conference on AIDS. Montreal, Canada, June 4-9, 1990, paper no. T.C.O.1.
-
(1990)
International Conference on AIDS
-
-
Belleau, B.1
Dixit, D.2
Nguyen-Ga, N.3
Kraus, J.-L.4
-
2
-
-
0025866982
-
Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog
-
Soudeyns, H.; Yao, Q.; Belleau, B.; Kraus, J.-L.; Nguyen-Ga, N.; Spira, B.; Wainberg, M. A. Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog. Antimicrob. Agents Chemother. 1991, 35, 1386-1390.
-
(1991)
Antimicrob. Agents Chemother.
, vol.35
, pp. 1386-1390
-
-
Soudeyns, H.1
Yao, Q.2
Belleau, B.3
Kraus, J.-L.4
Nguyen-Ga, N.5
Spira, B.6
Wainberg, M.A.7
-
3
-
-
0026058540
-
Inhibition of the replication of hepatitis B virus in vitro by 2′,3′-dideoxy-3′-thiacytidine and related analogues
-
Doong, S.-L.; Tsai, C. H.; Schinazi, R. F.; Liotta, D. C.; Cheng, Y.-C. Inhibition of the replication of hepatitis B virus in vitro by 2′,3′-dideoxy-3′-thiacytidine and related analogues. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 8495-8499.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 8495-8499
-
-
Doong, S.-L.1
Tsai, C.H.2
Schinazi, R.F.3
Liotta, D.C.4
Cheng, Y.-C.5
-
4
-
-
0026480950
-
Selective inhibition of human immunodeficiency viruses by racemates and enatiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-cytosine
-
Schinazi, R. F.; McMillan, A.; Cannon, D.; Mathis, R.; Lloyd, R. M.; Peck, A.; Sommadossi, J.-P.; St Clair, M.; Wilson, J.; Furman, P. A.; Painter, G.; Choi, W.-B.; Liotta, D. C. Selective inhibition of human immunodeficiency viruses by racemates and enatiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-cytosine. Antimicrob. Agents Chemother. 1992, 36, 2423-2431.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 2423-2431
-
-
Schinazi, R.F.1
McMillan, A.2
Cannon, D.3
Mathis, R.4
Lloyd, R.M.5
Peck, A.6
Sommadossi, J.-P.7
St Clair, M.8
Wilson, J.9
Furman, P.A.10
Painter, G.11
Choi, W.-B.12
Liotta, D.C.13
-
5
-
-
0026469165
-
The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl] cytosine
-
Furman, P. A.; Davis, M.; Liotta, D. C.; Paff, M.; Frick, L. W.; Nelson, D. J.; Dornsife, R. E.; Wurster, J. A.; Wilson, L. J.; Fyfe, J. A.; Tuttle, J. V.; Miller, W. H.; Condreay; L.; Averette, D. R.; Schinazi, R. F.; Painter, G. R. The anti-hepatitis B virus activities, cytotoxicities, and anabolic profiles of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl] cytosine. Antimicrob. Agents Chemother. 1992, 36, 2686-2692.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 2686-2692
-
-
Furman, P.A.1
Davis, M.2
Liotta, D.C.3
Paff, M.4
Frick, L.W.5
Nelson, D.J.6
Dornsife, R.E.7
Wurster, J.A.8
Wilson, L.J.9
Fyfe, J.A.10
Tuttle, J.V.11
Miller, W.H.12
Condreay, L.13
Averette, D.R.14
Schinazi, R.F.15
Painter, G.R.16
-
6
-
-
0028230923
-
Anti-human immunodeficiency virus activities of the β-L-enantiomer of 2′,3′-dideoxycytidine and its 5-fluoro derivative in vitro
-
Gosselin, G.; Schinazi, R. F.; Sommadossi, J.-P.; Mathe, C.; Bergogne, M.-C.; Aubertin, A.-M.; Kirn, A.; Imbach, J.-L. Anti-human immunodeficiency virus activities of the β-L-enantiomer of 2′,3′-dideoxycytidine and its 5-fluoro derivative in vitro. Antimicrob. Agents Chemother. 1994, 38, 1292-1297.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 1292-1297
-
-
Gosselin, G.1
Schinazi, R.F.2
Sommadossi, J.-P.3
Mathe, C.4
Bergogne, M.-C.5
Aubertin, A.-M.6
Kirn, A.7
Imbach, J.-L.8
-
7
-
-
0028212546
-
Synthesis and biological evaluation of 2′,3′-dideoxy-L-pyrimidine nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus (HBV)
-
Lin, T. S.; Luo, M. Z.; Pai, S. B.; Dutschuman, G. E.; Cheng, Y.-C. Synthesis and biological evaluation of 2′,3′-dideoxy-L-pyrimidine nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus (HBV). J. Med. Chem. 1994, 37, 798-803.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 798-803
-
-
Lin, T.S.1
Luo, M.Z.2
Pai, S.B.3
Dutschuman, G.E.4
Cheng, Y.-C.5
-
8
-
-
0001286905
-
Potent anti-HIV and anti-HBV activities of (-)-L-β-dioxolane-C and (+)-L-β-dioxolane-T and their asymmetric synthesis
-
Kim, H. O.; Shanmuganathan, K.; Alves, A. J.; Jeong, L. S.; Beach, J. W.; Schinazi, R. F.; Chang, C.-N.; Cheng, Y.-C, and Chu, C. K. Potent anti-HIV and anti-HBV activities of (-)-L-β-dioxolane-C and (+)-L-β-dioxolane-T and their asymmetric synthesis. Tetrahedron Lett. 1992, 33, 6899-6902.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 6899-6902
-
-
Kim, H.O.1
Shanmuganathan, K.2
Alves, A.J.3
Jeong, L.S.4
Beach, J.W.5
Schinazi, R.F.6
Chang, C.-N.7
Cheng, Y.-C.8
Chu, C.K.9
-
9
-
-
0028982940
-
Anticancer activity of β-L-dioxolane-cytidine, a novel nucleoside analogue with the unnatural L configuration
-
Grove, K. L.; Guo, X.; Liu, S.-H.; Gao, Z.; Chu, C. K.; Cheng, Y.-C. Anticancer activity of β-L-dioxolane-cytidine, a novel nucleoside analogue with the unnatural L configuration. Cancer Res. 1995, 55, 3008-3011.
-
(1995)
Cancer Res.
, vol.55
, pp. 3008-3011
-
-
Grove, K.L.1
Guo, X.2
Liu, S.-H.3
Gao, Z.4
Chu, C.K.5
Cheng, Y.-C.6
-
10
-
-
0028943355
-
Use of 2′-fluoro-5-methyl-β-L-arabinofuranosyluracil as a novel antiviral agent for hepatitis B virus and Epstein-Barr virus
-
Chu, C. K.; Ma, T. W.; Shanmuganathan, K.; Wang, C. G.; Xiang, Y. J.; Pai, S. B.; Yao, G. Q.; Sommadossi, J.-P.; Cheng, Y.-C. Use of 2′-fluoro-5-methyl-β-L-arabinofuranosyluracil as a novel antiviral agent for hepatitis B virus and Epstein-Barr virus. Antimicrob. Agents Chemother. 1995, 39, 979-981.
-
(1995)
Antimicrob. Agents Chemother.
, vol.39
, pp. 979-981
-
-
Chu, C.K.1
Ma, T.W.2
Shanmuganathan, K.3
Wang, C.G.4
Xiang, Y.J.5
Pai, S.B.6
Yao, G.Q.7
Sommadossi, J.-P.8
Cheng, Y.-C.9
-
11
-
-
0000226527
-
Mitochondrial toxicity of antiviral nucleoside analogues
-
Parker, W. B. and Cheng, Y.-C. Mitochondrial toxicity of antiviral nucleoside analogues. J. NIH Res. 1994, 6, 57-61.
-
(1994)
J. NIH Res.
, vol.6
, pp. 57-61
-
-
Parker, W.B.1
Cheng, Y.-C.2
-
12
-
-
0028817865
-
Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational analogue for chronic hepatitis B
-
McKenzie, R.; Fried, M. W.; Sallie, R.; ConJee Varam, H.; Di Bisceglie, A. M.; Park, Y.; Savarese, B.; Kleiner, D.; Tsokos, M.; Luciano, C.; Pruett, T.; Stotka, J. L.; Straus, S. E.; Hoofnagle, J.-H. Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational analogue for chronic hepatitis B. N. Engl. J. Med. 1995, 333, 1099-1105.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 1099-1105
-
-
McKenzie, R.1
Fried, M.W.2
Sallie, R.3
ConJee Varam, H.4
Di Bisceglie, A.M.5
Park, Y.6
Savarese, B.7
Kleiner, D.8
Tsokos, M.9
Luciano, C.10
Pruett, T.11
Stotka, J.L.12
Straus, S.E.13
Hoofnagle, J.-H.14
-
13
-
-
8944249316
-
-
Unpublished results
-
Cheng, Y.-C. Unpublished results.
-
-
-
Cheng, Y.-C.1
-
15
-
-
0030045732
-
Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β-L-arabinofuranosyluracil
-
Pai, S. B.; Liu, S.-H.; Zhu, Y.-L.; Chu, C. K; Cheng, Y.-C. Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β-L-arabinofuranosyluracil. Antimicrob. Agents Chemother. 1996, 40, 380-386.
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 380-386
-
-
Pai, S.B.1
Liu, S.-H.2
Zhu, Y.-L.3
Chu, C.K.4
Cheng, Y.-C.5
-
16
-
-
0022341203
-
Fluorocarbohydrates in synthesis. An efficient synthesis of 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil (β-FIAU) and 1-(2-deoxy-2-fluoro-β-d-arabinofuranosyl) thymine (β-FMAU)
-
Tann, C. H.; Brodfuehrer, P. R.; Brundidge, S. P.; Sapino, C., Jr.; Howell, H. G. Fluorocarbohydrates in synthesis. An efficient synthesis of 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil (β-FIAU) and 1-(2-deoxy-2-fluoro-β-d-arabinofuranosyl) thymine (β-FMAU). J. Org. Chem. 1985, 50, 3644-3646
-
(1985)
J. Org. Chem.
, vol.50
, pp. 3644-3646
-
-
Tann, C.H.1
Brodfuehrer, P.R.2
Brundidge, S.P.3
Sapino Jr., C.4
Howell, H.G.5
-
17
-
-
0008837982
-
A new synthesis of L-ribofuranose derivatives
-
Walker, T. E.; Hagenkamp, H. P. C. A new synthesis of L-ribofuranose derivatives. Carbohydr. Res. 1974, 32, 413-417.
-
(1974)
Carbohydr. Res.
, vol.32
, pp. 413-417
-
-
Walker, T.E.1
Hagenkamp, H.P.C.2
-
18
-
-
2042417635
-
9-β-L-ribofuranosyladenine (L-adenosine), configurational inversion within a furanoid ring
-
Zorbach, W. W., Tipson, R. S., Eds.; Wiley: New York
-
Kenneth, J. R.; Edward, M. A. 9-β-L-ribofuranosyladenine (L-adenosine), configurational inversion within a furanoid ring. In Synthetic Procedures in Nucleic Acids Chemistry, V. 1; Zorbach, W. W., Tipson, R. S., Eds.; Wiley: New York, 1968; pp 163-167.
-
(1968)
Synthetic Procedures in Nucleic Acids Chemistry
, vol.1
, pp. 163-167
-
-
Kenneth, J.R.1
Edward, M.A.2
-
19
-
-
85011247445
-
Epimerization of aldoses catalyzed by dioxobis (2,4-pentanedionato-o,o′)-molybdenum (VI). An improved procedure for C-2 epimer preparation
-
Abe, Y.; Takizawa, T.; Kunieda, T. Epimerization of aldoses catalyzed by dioxobis (2,4-pentanedionato-o,o′)-molybdenum (VI). An improved procedure for C-2 epimer preparation. Chem. Pharm. Bull. 1980, 28 (4), 1324-1326.
-
(1980)
Chem. Pharm. Bull.
, vol.28
, Issue.4
, pp. 1324-1326
-
-
Abe, Y.1
Takizawa, T.2
Kunieda, T.3
-
20
-
-
21844514964
-
New synthesis of L-ribofuranose derivatives
-
Batch, A.; Czernecki, S. New synthesis of L-ribofuranose derivatives. J. Carbohydr. Chem. 1994, 13 (6), 935-940.
-
(1994)
J. Carbohydr. Chem.
, vol.13
, Issue.6
, pp. 935-940
-
-
Batch, A.1
Czernecki, S.2
-
21
-
-
0040310207
-
Synthesis of D-ribose from D-xylose
-
Oka, K.; Wada, H. Synthesis of D-ribose from D-xylose. Yakugaku Zasshi. 1963, 83, 890-891; Chem. Abstr. 1964, 60, 1825d.
-
(1963)
Yakugaku Zasshi.
, vol.83
, pp. 890-891
-
-
Oka, K.1
Wada, H.2
-
22
-
-
0040310207
-
-
Oka, K.; Wada, H. Synthesis of D-ribose from D-xylose. Yakugaku Zasshi. 1963, 83, 890-891; Chem. Abstr. 1964, 60, 1825d.
-
(1964)
Chem. Abstr.
, vol.60
-
-
-
23
-
-
0001989139
-
1,2-Di-O-acetyl-3,5-di-O-benzoyl-D-xylofuranose, a versatile precursor for the synthesis of various β-D-pentofuranosyl nucleosides and related analogs
-
Townsend, L. B., Tipson, R. S., Eds.; Wiley: New York
-
Gosselin, G.; Bergogne, M.-C.; Imbach, J.-L. 1,2-Di-O-acetyl-3,5-di-O-benzoyl-D-xylofuranose, a versatile precursor for the synthesis of various β-D-pentofuranosyl nucleosides and related analogs. In Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 4; Townsend, L. B., Tipson, R. S., Eds.; Wiley: New York, 1991; pp 41-45.
-
(1991)
Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 4
, pp. 41-45
-
-
Gosselin, G.1
Bergogne, M.-C.2
Imbach, J.-L.3
-
24
-
-
0005518994
-
Base-catalyzed degradations of carbohydrates. IV. Formation of 2,3-anhydro-2-methyl-α-D-allopyranose derivatives from 3-deoxy-D-erythro-hex-2-enopyranoses
-
Aspinall, G. O.; King, R. R. Base-catalyzed degradations of carbohydrates. IV. Formation of 2,3-anhydro-2-methyl-α-D-allopyranose derivatives from 3-deoxy-D-erythro-hex-2-enopyranoses. Can. J. Chem. 1973, 51, 394-401.
-
(1973)
Can. J. Chem.
, vol.51
, pp. 394-401
-
-
Aspinall, G.O.1
King, R.R.2
-
25
-
-
0027686257
-
1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose, a versatile precursor for the synthesis of 3-deoxy-3-fluoro-β-D-xylofuranosyl nucleosides as potential antiviral agents
-
Gosselin, G.; Puech, F.; Genu-Dellac, C.; Imbach, J. L. 1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose, a versatile precursor for the synthesis of 3-deoxy-3-fluoro-β-D-xylofuranosyl nucleosides as potential antiviral agents. Carbohydr. Res. 1993, 249, 1-17.
-
(1993)
Carbohydr. Res.
, vol.249
, pp. 1-17
-
-
Gosselin, G.1
Puech, F.2
Genu-Dellac, C.3
Imbach, J.L.4
-
26
-
-
21844511513
-
New synthesis of L-ribofuranose derivatives from L-xylose
-
After we completed the research work for this paper, a similar methodology for the synthesis of compound 6 was recently reported in the literature. Chelain, E.; Floch, O.; Czernecki, S. New synthesis of L-ribofuranose derivatives from L-xylose. J. Carbohydr. Chem. 1995, 14, 1251-1256.
-
(1995)
J. Carbohydr. Chem.
, vol.14
, pp. 1251-1256
-
-
Chelain, E.1
Floch, O.2
Czernecki, S.3
-
27
-
-
1842287251
-
2′-O-methyl nucleosides, stereospecific synthesis via a readily available 2′-O-methylated ribofuranose derivative
-
Townsend, L. B., Tipson, R. S., Eds.; Wiley: New York
-
Chavis, C.; Dumont, F.; Wightman, R.; Ziegler, J.-C.; Imbach, J.-L. 2′-O-methyl nucleosides, stereospecific synthesis via a readily available 2′-O-methylated ribofuranose derivative. In Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 3; Townsend, L. B., Tipson, R. S., Eds.; Wiley: New York, 1986; pp 76-80.
-
(1986)
Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 3
, pp. 76-80
-
-
Chavis, C.1
Dumont, F.2
Wightman, R.3
Ziegler, J.-C.4
Imbach, J.-L.5
-
28
-
-
0030066252
-
Triethylamine poly(hydrogen fluorides) in the synthesis of a fluorinated nucleoside glycon
-
Chou, T. S.; Becke, L. M.; O'Toole, J. C.; Carr, M. A.; Parker, B. E. Triethylamine poly(hydrogen fluorides) in the synthesis of a fluorinated nucleoside glycon. Tetrahedron. Lett. 1996, 37, 17-20.
-
(1996)
Tetrahedron. Lett.
, vol.37
, pp. 17-20
-
-
Chou, T.S.1
Becke, L.M.2
O'Toole, J.C.3
Carr, M.A.4
Parker, B.E.5
-
29
-
-
0002642858
-
Antiviral Nucleosides. A stereospecific, total synthesis of 2′-fluoro-2′-deoxy-β-D-arabinofuranosyl nucleosides
-
and references cited therein
-
Howell, H. G.; Brodfuehreu, P. R.; Brundidge, S. P.; Benigni, D. A.; Sapino, C., Jr. Antiviral Nucleosides. A stereospecific, total synthesis of 2′-fluoro-2′-deoxy-β-D-arabinofuranosyl nucleosides. J. Org. Chem. 1988, 53, 85-88 and references cited therein.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 85-88
-
-
Howell, H.G.1
Brodfuehreu, P.R.2
Brundidge, S.P.3
Benigni, D.A.4
Sapino Jr., C.5
-
30
-
-
27544440920
-
Nucleic acid related compounds. 39. Efficient conversion of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides
-
Robins, M. J.; Barr, P. J. Nucleic acid related compounds. 39. Efficient conversion of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides. J. Org. Chem. 1983, 48, 1854-1862.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 1854-1862
-
-
Robins, M.J.1
Barr, P.J.2
-
31
-
-
85009838308
-
E- and Z-5-(2-bromovinyl)-2′-deoxyuridine, a potent anti-herpes virus agent (E-isomer) and its diastereoisomer (Z-isomer)
-
Townsend, L. B., Tipson, R. S., Eds.; John Wiley & Sons, Inc.: New York
-
Jones, A. S.; Rahim, S. G.; Verhelst, G.; Walker, R. T. E- and Z-5-(2-bromovinyl)-2′-deoxyuridine, a potent anti-herpes virus agent (E-isomer) and its diastereoisomer (Z-isomer). In Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 3; Townsend, L. B., Tipson, R. S., Eds.; John Wiley & Sons, Inc.: New York, 1986; pp 61-64.
-
(1986)
Nucleic Acid Chemistry, Improved and New Synthetic Procedures, Methods and Techniques, Part 3
, pp. 61-64
-
-
Jones, A.S.1
Rahim, S.G.2
Verhelst, G.3
Walker, R.T.4
-
32
-
-
0018331237
-
Nucleosides. 110. Synthesis and antiherpes virus activity of some 2′-fluoro-2′-deoxy-arabinofuranosylpyrimidine nucleosides
-
Watanabe, K. A.; Reichman, U.; Hirota, K.; Lopez, C.; Fox, J. J. Nucleosides. 110. Synthesis and antiherpes virus activity of some 2′-fluoro-2′-deoxy-arabinofuranosylpyrimidine nucleosides. J. Med. Chem. 1979, 22, 21-24.
-
(1979)
J. Med. Chem.
, vol.22
, pp. 21-24
-
-
Watanabe, K.A.1
Reichman, U.2
Hirota, K.3
Lopez, C.4
Fox, J.J.5
-
33
-
-
0021288411
-
Nucleosides. 129. Synthesis of antiviral nucleosides, 5-alkenyl-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)uracils
-
Watanabe, K. A.; Su, T.-L.; Reichman, U.; Greenberg, N.; Lopez, C.; Fox, J. J. Nucleosides. 129. Synthesis of antiviral nucleosides, 5-alkenyl-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)uracils. J. Med. Chem. 1984, 27, 91-94.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 91-94
-
-
Watanabe, K.A.1
Su, T.-L.2
Reichman, U.3
Greenberg, N.4
Lopez, C.5
Fox, J.J.6
-
34
-
-
0020662793
-
Nucleosides. 123. Synthesis of antiviral nucleosides, 5-substituted 1-(2-deoxy-2-halogeno-β-D-arabinofuranosyl) cytosines and uracils, some structure-activity relationships
-
Watanabe, K. A.; Su, T.-L.; Klein, R. S.; Chu, C. K.; Matsuda, A.; Chun, M. W.; Lopez, C.; Fox, J. J. Nucleosides. 123. Synthesis of antiviral nucleosides, 5-substituted 1-(2-deoxy-2-halogeno-β-D-arabinofuranosyl) cytosines and uracils, some structure-activity relationships. J. Med. Chem. 1983, 26, 152-156.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 152-156
-
-
Watanabe, K.A.1
Su, T.-L.2
Klein, R.S.3
Chu, C.K.4
Matsuda, A.5
Chun, M.W.6
Lopez, C.7
Fox, J.J.8
-
35
-
-
0023926234
-
Synthesis and anti- Herpetic activity of a 2′-fluoroarabinosyl analog of trifluridine
-
Smee, D. F.; Chernow, M.; Kraft, M.; Okamoto, P. M.; Prisbe, E. J. Synthesis and anti- herpetic activity of a 2′-fluoroarabinosyl analog of trifluridine. Nucleosides Nucleotides. 1988, 7, 155-165.
-
(1988)
Nucleosides Nucleotides.
, vol.7
, pp. 155-165
-
-
Smee, D.F.1
Chernow, M.2
Kraft, M.3
Okamoto, P.M.4
Prisbe, E.J.5
-
36
-
-
0026021189
-
13C NMR method to assign regio- and stereochemistry of 2′-deoxy-2′-fluoroarabinofuranosyl nucleosides
-
13C NMR method to assign regio- and stereochemistry of 2′-deoxy-2′-fluoroarabinofuranosyl nucleosides. Tetrahedron Lett. 1991, 1287-1290.
-
(1991)
Tetrahedron Lett.
, pp. 1287-1290
-
-
Mansuri, M.M.1
Krishnan, B.2
Martin, J.C.3
-
37
-
-
8944232126
-
-
note
-
1 (No. 4), Z = 4. There are two molecules in the asymmetric unit.
-
-
-
-
38
-
-
0024514375
-
Compact organization of the hepatitis B virus genome
-
Miller, R. H.; Kaneko, S.; Chung, C. T.; Girones, R.; Purcell, R. H. Compact organization of the hepatitis B virus genome. Hepatology 1989, 9, 322-327.
-
(1989)
Hepatology
, vol.9
, pp. 322-327
-
-
Miller, R.H.1
Kaneko, S.2
Chung, C.T.3
Girones, R.4
Purcell, R.H.5
-
39
-
-
0029031381
-
Mechanism of inhibition of duck hepatitis B virus polymerase by (-)-β-L-2′,3′-dideoxy-3′-thiacytidine
-
Severini, A.; Liu, X.-Y.; Wilson, J. S.; Tyrrell, D. L. J. Mechanism of inhibition of duck hepatitis B virus polymerase by (-)-β-L-2′,3′-dideoxy-3′-thiacytidine. Antimicrob. Agents Chemother. 1995, 39, 1430-1435.
-
(1995)
Antimicrob. Agents Chemother.
, vol.39
, pp. 1430-1435
-
-
Severini, A.1
Liu, X.-Y.2
Wilson, J.S.3
Tyrrell, D.L.J.4
-
40
-
-
0001051248
-
New benzoyl derivatives of D-ribofuranose and aldehydo-D-ribose. The preparation of crystalline 2,3,5-tri-O-benzoyl-β-D-ribose from D-ribose
-
Ness, R. K.; Diehl, H. W.; Fletcher, H. G., Jr. New benzoyl derivatives of D-ribofuranose and aldehydo-D-ribose. The preparation of crystalline 2,3,5-tri-O-benzoyl-β-D-ribose from D-ribose. J. Am. Chem. Soc. 1954, 76, 763-767.
-
(1954)
J. Am. Chem. Soc.
, vol.76
, pp. 763-767
-
-
Ness, R.K.1
Diehl, H.W.2
Fletcher Jr., H.G.3
|