-
1
-
-
0017166941
-
4′-substituted nucleosides. 3. Synthesis of some 4′-fluorouridine derivatives
-
(a) Owen, G. R.; Verheyden, J. P. H.; Moffatt, J. G. 4′ -Substituted nucleosides. 3. Synthesis of some 4′-fluorouridine derivatives. J. Org. Chem. 1976, 41, 3010-3017.
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3010-3017
-
-
Owen, G.R.1
Verheyden, J.P.H.2
Moffatt, J.G.3
-
2
-
-
0025218997
-
Acid-stable 2′-fluoro purine dideoxynucleosides as active agents against HIV
-
(b) Marquez, V. E.; Tseng, C. K.-H.; Mitsuya, H.; Aoki, S.; Kelley, J. A.; Ford, H., Jr.; Roth, J. S.; Broder, S.; Johns, D. G.; Driscoll, J. S. Acid-stable 2′-fluoro purine dideoxynucleosides as active agents against HIV. J. Med. Chem. 1990, 33, 978-985.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 978-985
-
-
Marquez, V.E.1
Tseng, C.K.-H.2
Mitsuya, H.3
Aoki, S.4
Kelley, J.A.5
Ford Jr., H.6
Roth, J.S.7
Broder, S.8
Johns, D.G.9
Driscoll, J.S.10
-
3
-
-
0030045732
-
Inhibition of hepatitis B virus by a novel L-nucleoside, 2′-fluoro-5-methyl-β-L-arabinofuranosyluracil
-
(c) 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
-
4
-
-
0033535597
-
Synthesis and anti-HIV and anti-HBV activities of 2′ -fluoro-2′,3′-unsaturated L-nucleosides
-
(d) Lee, K.; Choi, Y.; Gullen, E.; Schlueter-Wirtz, S.; Schinazi, R. F.; Cheng, Y.-C.; Chu, C. K. Synthesis and anti-HIV and anti-HBV activities of 2′-fluoro-2′,3′-unsaturated L-nucleosides. J. Med. Chem. 1999, 42, 1320-1328.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1320-1328
-
-
Lee, K.1
Choi, Y.2
Gullen, E.3
Schlueter-Wirtz, S.4
Schinazi, R.F.5
Cheng, Y.-C.6
Chu, C.K.7
-
5
-
-
0034675036
-
Synthesis of 2′,3′-dideoxy-3′-fluoro-L-ribonucleosides as potential antiviral agents from D-sorbitol
-
(e) Chun, B. K.; Schinazi, R. F.; Cheng, Y.-C.; Chu, C. K. Synthesis of 2′,3′-dideoxy-3′-fluoro-L-ribonucleosides as potential antiviral agents from D-sorbitol. Carbohydr. Res. 2000, 328, 49-59.
-
(2000)
Carbohydr. Res.
, vol.328
, pp. 49-59
-
-
Chun, B.K.1
Schinazi, R.F.2
Cheng, Y.-C.3
Chu, C.K.4
-
6
-
-
0000306137
-
Synthesis of 4-thio-D- & L-ribofuranose and corresponding adenine nucleosides
-
(a) Reist, E. J.; Gueffroy, D. E.; Goodman, L. Synthesis of 4-thio-D- & L-ribofuranose and corresponding adenine nucleosides. J. Am. Chem. Soc. 1964, 86, 5658-5663.
-
(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 5658-5663
-
-
Reist, E.J.1
Gueffroy, D.E.2
Goodman, L.3
-
7
-
-
0014231434
-
Neighboring-group participation. Preparation of dithiopentose sugars via a thioacylonium ion intermediate
-
(b) Reist, E. J.; Fisher, L. V.; Gueffroy, E.; Goodman, L. Neighboring-group participation. Preparation of dithiopentose sugars via a thioacylonium ion intermediate. J. Org. Chem. 1968, 33, 189-192.
-
(1968)
J. Org. Chem.
, vol.33
, pp. 189-192
-
-
Reist, E.J.1
Fisher, L.V.2
Gueffroy, E.3
Goodman, L.4
-
8
-
-
0015223917
-
4-Thio-D-arabinofuranosylpyrimidine nucleosides
-
(a) Whistler, R. L.; Doner, L. W.; Nayak, U. G. 4-Thio-D-arabinofuranosylpyrimidine nucleosides. J. Org. Chem. 1971, 36, 108-110.
-
(1971)
J. Org. Chem.
, vol.36
, pp. 108-110
-
-
Whistler, R.L.1
Doner, L.W.2
Nayak, U.G.3
-
9
-
-
0016723031
-
Synthesis and biological activity of 5-fluoro-4′-thiouridine and some related nucleosides
-
(b) Bobek, M.; Bloch, A.; Parthasarathy, R.; Whistler, R. L. Synthesis and biological activity of 5-fluoro-4′-thiouridine and some related nucleosides. J. Med. Chem. 1975, 18, 784-787.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 784-787
-
-
Bobek, M.1
Bloch, A.2
Parthasarathy, R.3
Whistler, R.L.4
-
10
-
-
0016366112
-
Preparation and antitumor activity of 4′-thio analogs of 2,2′-anhydro-1-β-D-arabinofuranosylcytosine
-
(c) Ototani, N.; Whistler, R. L. Preparation and antitumor activity of 4′-thio analogs of 2,2′-anhydro-1-β-D-arabinofuranosylcytosine. J. Med. Chem. 1974, 17, 535-537.
-
(1974)
J. Med. Chem.
, vol.17
, pp. 535-537
-
-
Ototani, N.1
Whistler, R.L.2
-
11
-
-
0011125471
-
-
Townsend, L.; Tipson, R. S., Eds.; John Wiley & Sons: New York
-
(d) Fu, Y.-L.; Bobek, M. In Nucleic Aicd Chemistry; Townsend, L.; Tipson, R. S., Eds.; John Wiley & Sons: New York, 1978; pp 317-323.
-
(1978)
Nucleic Aicd Chemistry
, pp. 317-323
-
-
Fu, Y.-L.1
Bobek, M.2
-
12
-
-
0025827985
-
The synthesis and antiviral properties of E-5-(2-bromovinyl)-4′ -thio-2′-deoxyuridine
-
(a) Dyson, M. R.; Coe, P. L.; Walker, R. T. The synthesis and antiviral properties of E-5-(2-bromovinyl)-4′-thio-2′-deoxyuridine. J. Chem. Soc., Chem. Commun. 1991, 741-742.
-
(1991)
J. Chem. Soc., Chem. Commun.
, pp. 741-742
-
-
Dyson, M.R.1
Coe, P.L.2
Walker, R.T.3
-
13
-
-
0026012222
-
The synthesis and antiviral activity of some 4′-thio-2′ -deoxy nucleoside analogs
-
(b) Dyson, M. R.; Coe, P. L.; Walker, R. T. The synthesis and antiviral activity of some 4′-thio-2′-deoxy nucleoside analogs. J. Med. Chem. 1991, 34, 2782-2786.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2782-2786
-
-
Dyson, M.R.1
Coe, P.L.2
Walker, R.T.3
-
14
-
-
0026045160
-
Synthesis and biological activity of 2′-deoxy-4′ -thiopyrimidine nucleosides
-
(c) Secrist, J. A.; Tiwari, K. N.; Riordan, J. M.; Montgomery, J. A. Synthesis and biological activity of 2′-deoxy-4′-thiopyrimidine nucleosides. J. Med. Chem. 1991, 34, 2361-2366.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2361-2366
-
-
Secrist, J.A.1
Tiwari, K.N.2
Riordan, J.M.3
Montgomery, J.A.4
-
15
-
-
0026095737
-
Stereocontrolled preparation of cyclic xanthate - A novel synthetic route to 4-thiofuranose and 4′-thionucleoside
-
(d) Uenishi, J.; Motoyama, M.; Nishiyama, Y.; Wakabayashi, S. Stereocontrolled preparation of cyclic xanthate-A novel synthetic route to 4-thiofuranose and 4′-thionucleoside. J. Chem. Soc., Chem. Commun. 1991, 1421-1422.
-
(1991)
J. Chem. Soc., Chem. Commun.
, pp. 1421-1422
-
-
Uenishi, J.1
Motoyama, M.2
Nishiyama, Y.3
Wakabayashi, S.4
-
16
-
-
0028245909
-
Syntheses and antitumor activities of D-2′-deoxy-4′-thio and L-2′-deoxy-4′-thio pyrimidine nucleosides
-
(e) Uenishi, J.; Takahashi, K.; Motoyama, M.; Akashi, H.; Sasaki, T. Syntheses and antitumor activities of D-2′-deoxy-4′-thio and L-2′-deoxy-4′-thio pyrimidine nucleosides. Nucleosides Nucleotides 1994, 13, 1347-1361.
-
(1994)
Nucleosides Nucleotides
, vol.13
, pp. 1347-1361
-
-
Uenishi, J.1
Takahashi, K.2
Motoyama, M.3
Akashi, H.4
Sasaki, T.5
-
17
-
-
0026551053
-
Synthesis and anti-HIV activity of 4′-thio-2′,3′ -dideoxynucleosides
-
(f) Secrist, J. A.; Riggs, R. M.; Tiwari, K. N.; Montgomery, J. A. Synthesis and anti-HIV activity of 4′-thio-2′,3′ -dideoxynucleosides. J. Med. Chem. 1992, 35, 533-538.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 533-538
-
-
Secrist, J.A.1
Riggs, R.M.2
Tiwari, K.N.3
Montgomery, J.A.4
-
18
-
-
0032563960
-
Synthesis and biological activity of certain 4′ -thio-D-arabinofuranosylpurine nucleosides
-
(g) Secrist, J. A.; Tiwari, K. N.; Shortnacy-Fowler, A. T.; Messini, L.; Riordan, J. M.; Montgomery, J. A. Synthesis and biological activity of certain 4′-thio-D-arabinofuranosylpurine nucleosides. J. Med. Chem. 1998, 41, 3865-3871.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3865-3871
-
-
Secrist, J.A.1
Tiwari, K.N.2
Shortnacy-Fowler, A.T.3
Messini, L.4
Riordan, J.M.5
Montgomery, J.A.6
-
19
-
-
0030803389
-
A facile, alternative synthesis of 4′-thioarabinonucleosides and their biological activities
-
(h) Yoshimura, Y.; Watanabe, M.; Satoh, H.; Ashida, N.; Ijichi, K.; Sakata, S.; Machida, H.; Matsuda, A. A facile, alternative synthesis of 4′-thioarabinonucleosides and their biological activities. J. Med. Chem. 1997, 40, 2177-2183.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2177-2183
-
-
Yoshimura, Y.1
Watanabe, M.2
Satoh, H.3
Ashida, N.4
Ijichi, K.5
Sakata, S.6
Machida, H.7
Matsuda, A.8
-
20
-
-
0030917732
-
A novel synthesis of 2′-modified 2′-deoxy-4′ -thiocytidines from D-glucose
-
(i) Yoshimura, Y.; Kitano, K.; Yamada, K.; Satoh, H.; Watanabe, M.; Miura, S.; Sakata, S.; Sasaki, T.; Matsuda, A. A novel synthesis of 2′-modified 2′-deoxy-4′-thiocytidines from D-glucose. J. Org. Chem. 1997, 62, 3140-3152.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3140-3152
-
-
Yoshimura, Y.1
Kitano, K.2
Yamada, K.3
Satoh, H.4
Watanabe, M.5
Miura, S.6
Sakata, S.7
Sasaki, T.8
Matsuda, A.9
-
21
-
-
0002053132
-
-
Sartorelli, A, C., Lazo, J. S., Bertino, J. R., Eds.; Academic Press: New York
-
(j) Parks, R. E., Jr.; Stoeckler, J. D.; Cambor, C.; Savarese, T. M.; Crabtree, G. W.; Chu, S.-H. In Molecular Actions and Targets for Cancer Chemotherapeutic Agents; Sartorelli, A. C., Lazo, J. S., Bertino, J. R., Eds.; Academic Press: New York, 1981; pp 229-252.
-
(1981)
Molecular Actions and Targets for Cancer Chemotherapeutic Agents
, pp. 229-252
-
-
Parks Jr., R.E.1
Stoeckler, J.D.2
Cambor, C.3
Savarese, T.M.4
Crabtree, G.W.5
Chu, S.-H.6
-
22
-
-
0028811637
-
Synthesis and antiviral evaluation of enantiomeric 2′,3′ -dideoxy- and 2′,3′-didehydro-2′,3′-dideoxy-4′ -thionucleosides
-
Young, R. J.; Shaw-Ponter, S.; Thomson, J. B.; Miller, J. A.; Cumming, J. G.; Pugh, A. W.; Rider, P. Synthesis and antiviral evaluation of enantiomeric 2′,3′-dideoxy- and 2′,3′-didehydro-2′,3′ -dideoxy-4′-thionucleosides. Bioorg. Med. Chem. Lett. 1995, 5, 2599-2604.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2599-2604
-
-
Young, R.J.1
Shaw-Ponter, S.2
Thomson, J.B.3
Miller, J.A.4
Cumming, J.G.5
Pugh, A.W.6
Rider, P.7
-
23
-
-
0037165411
-
Synthesis and potent anti-HIV activity of L-2′,3′ -didehydro-2′,3′-dideoxy-2′-fluoro-4′-thiocytidine
-
(a) Choi, Y.; Choo, H.; Chong, Y.; Lee, S.; Olgen, S.; Schinazi, R. F.; Chu, C. K. Synthesis and potent anti-HIV activity of L-2′,3′ -didehydro-2′,3′-dideoxy-2′-fluoro-4′-thiocytidine. Org. Lett. 2002, 4, 305-307.
-
(2002)
Org. Lett.
, vol.4
, pp. 305-307
-
-
Choi, Y.1
Choo, H.2
Chong, Y.3
Lee, S.4
Olgen, S.5
Schinazi, R.F.6
Chu, C.K.7
-
24
-
-
0037168035
-
Stereoselective synthesis and antiviral activities of D-2′,3′-didehydro-2′,3′-dideoxy-2′-fluoro-4′ -thionucleosides
-
(b) Chong, Y.; Choo, H.; Lee, S.; Choi, Y.; Schinazi, R. F.; Chu, C. K. Stereoselective synthesis and antiviral activities of D-2′,3′ -didehydro-2′,3′-dideoxy-2′-fluoro-4′-thionucleosides. J. Med. Chem. 2002, 45, 4888-4898.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4888-4898
-
-
Chong, Y.1
Choo, H.2
Lee, S.3
Choi, Y.4
Schinazi, R.F.5
Chu, C.K.6
-
25
-
-
0037472859
-
Synthesis, anti-HIV activity, and molecular mechanism of drug resistance of L-2′,3′-didehydro-2′,3′-dideoxy-2′ -fluoro-4′-thionucleosides
-
(c) Choo, H.; Chong, Y.; Choi, Y.; Mathew, J.; Schinazi, R. F.; Chu, C. K. Synthesis, anti-HIV activity, and molecular mechanism of drug resistance of L-2′,3′-didehydro-2′,3′-dideoxy-2′-fluoro-4′ -thionucleosides. J. Med. Chem. 2003, 46, 389-398.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 389-398
-
-
Choo, H.1
Chong, Y.2
Choi, Y.3
Mathew, J.4
Schinazi, R.F.5
Chu, C.K.6
-
26
-
-
0002053132
-
-
Sartorelli, A, C., Lazo, J. S., Bertino, J. R., Eds.; Academic Press: New York
-
Parks, R. E., Jr.; Stoeckler, J. D.; Cambor, C.; Savarese, T. M.; Crabtree, G. W.; Chu, S.-H. In Molecular Actions and Targets for Cancer Chemotherapeutic Agents; Sartorelli, A. C., Lazo, J. S., Bertino, J. R., Eds.; Academic Press: New York, 1981; pp 229-252.
-
(1981)
Molecular Actions and Targets for Cancer Chemotherapeutic Agents
, pp. 229-252
-
-
Parks Jr., R.E.1
Stoeckler, J.D.2
Cambor, C.3
Savarese, T.M.4
Crabtree, G.W.5
Chu, S.-H.6
-
27
-
-
0021019292
-
Phosphorolysis of (E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU) and other 5-substituted-2′-deoxyuridines by purified human thymidine phosphorylase and intact blood-platelets
-
(a) Desgranges, C.; Razaka, G.; Rabaud, M.; Bricaud, H.; Balzarini, J.; De Clercq, E. Phosphorolysis of (E)-5-(2-bromovinyl)-2′-deoxyuridine (BVDU) and other 5-substituted-2′-deoxyuridines by purified human thymidine phosphorylase and intact blood-platelets. Biochem. Pharmacol. 1983, 32, 3583-3590.
-
(1983)
Biochem. Pharmacol.
, vol.32
, pp. 3583-3590
-
-
Desgranges, C.1
Razaka, G.2
Rabaud, M.3
Bricaud, H.4
Balzarini, J.5
De Clercq, E.6
-
28
-
-
0022577593
-
Pharmacokinetics and metabolism of E-5-(2-[I-131]iodovinyl)-2′ -deoxyuridine in dogs
-
(b) Samuel, J.; Gill, M. J.; Iwashina, T.; Tovell, D. R.; Tyrrell, D. L. ; Knaus, E. E.; Wiebe, L. I. Pharmacokinetics and metabolism of E-5-(2-[I-131]iodovinyl)-2′-deoxyuridine in dogs. Antimicrob. Agents Chemother. 1986, 29, 320-324.
-
(1986)
Antimicrob. Agents Chemother.
, vol.29
, pp. 320-324
-
-
Samuel, J.1
Gill, M.J.2
Iwashina, T.3
Tovell, D.R.4
Tyrrell, D.L.5
Knaus, E.E.6
Wiebe, L.I.7
-
29
-
-
0035961051
-
Synthesis and potent anti-HIV activity of L-3′-fluoro-2′ ,3′-unsaturated cytidine
-
(a) Gunima, G.; Schinazi, R. F.; Chu, C. K. Synthesis and potent anti-HIV activity of L-3′-fluoro-2′,3′-unsaturated cytidine. Org. Lett. 2001, 3, 4177-4180.
-
(2001)
Org. Lett.
, vol.3
, pp. 4177-4180
-
-
Gunima, G.1
Schinazi, R.F.2
Chu, C.K.3
-
30
-
-
0038155280
-
L-2′,3′-Didehydro-2′,3′-dideoxy-3′ -fluoronucleosides: Synthesis, Anti-HIV Activity, Chemical and Enzymatic Stability and the Mechanism of Resistance
-
in press
-
(b) Chong, Y.; Gumina, G.; Mathew, J.; Schinazi, R. F.; Chu, C. K. L-2′,3′-Didehydro-2′,3′-dideoxy-3′ -fluoronucleosides: Synthesis, Anti-HIV Activity, Chemical and Enzymatic Stability and the Mechanism of Resistance. J. Med. Chem., in press.
-
J. Med. Chem.
-
-
Chong, Y.1
Gumina, G.2
Mathew, J.3
Schinazi, R.F.4
Chu, C.K.5
-
31
-
-
0024474384
-
3′-fluoro-2′,3′-dideoxy-5-chlorouridine: Most selective anti-HIV-1 agent among a series of new 2′- and 3′-fluorinated 2′,3′-dideoxynucleoside analogs
-
(a) Van Aerschot, A. V.; Herdewijn, P.; Balzarini, J.; Pauwels, R.; De Clercq, E. 3′-Fluoro-2′,3′-dideoxy-5-chlorouridine: most selective anti-HIV-1 agent among a series of new 2′- and 3′-fluorinated 2′,3′-dideoxynucleoside analogs. J. Med. Chem. 1989, 32, 1743-1749.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 1743-1749
-
-
Van Aerschot, A.V.1
Herdewijn, P.2
Balzarini, J.3
Pauwels, R.4
De Clercq, E.5
-
32
-
-
0024377037
-
Structure-activity relationships of fluorinated nucleoside analogs and their synergistic effect in combination with phsophonofornate against human immunodeficiency virus type 1
-
(b) Koshida, R.; Cox, S.; Harmenberg, J.; Gilljam, G.; Wahren, B. Structure-activity relationships of fluorinated nucleoside analogs and their synergistic effect in combination with phsophonofornate against human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 1989, 33, 2083-2088.
-
(1989)
Antimicrob. Agents Chemother.
, vol.33
, pp. 2083-2088
-
-
Koshida, R.1
Cox, S.2
Harmenberg, J.3
Gilljam, G.4
Wahren, B.5
-
33
-
-
0028283367
-
3′-C-phosphonates as nucleotide analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo-series)
-
(a) Serra, C.; Dewynter, W.; Montero, J.-L.; Imbach, J.-L. 3′-C-Phosphonates as nucleotide analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo-series). Tetrahedron 1994, 50, 8427-8444.
-
(1994)
Tetrahedron
, vol.50
, pp. 8427-8444
-
-
Serra, C.1
Dewynter, W.2
Montero, J.-L.3
Imbach, J.-L.4
-
34
-
-
0002880232
-
Stereochemical control as a function of protecting group participation in 2-deoxy-D-erythro-pentofuranosyl nucleosides
-
(b) Wierenga, W.; Skulnick, H. I. Stereochemical control as a function of protecting group participation in 2-deoxy-D-erythro-pentofuranosyl nucleosides. Carbohyd. Res. 1981, 90, 41-52.
-
(1981)
Carbohyd. Res.
, vol.90
, pp. 41-52
-
-
Wierenga, W.1
Skulnick, H.I.2
-
35
-
-
33847800447
-
New fluorinating reagents: Dialkylamino-sulfur fluorides
-
(a) Middleton, W. J. New fluorinating reagents: dialkylamino-sulfur fluorides. J. Org. Chem. 1975, 40, 574-578.
-
(1975)
J. Org. Chem.
, vol.40
, pp. 574-578
-
-
Middleton, W.J.1
-
36
-
-
0017817109
-
New approaches to the synthesis of 3-deoxy-3-fluoro-D-glucose
-
(b) Tewson, T. J.; Welch, M. J. New approaches to the synthesis of 3-deoxy-3-fluoro-D-glucose. J. Org. Chem. 1978, 43, 1090-1092.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 1090-1092
-
-
Tewson, T.J.1
Welch, M.J.2
-
37
-
-
0000883321
-
A short and efficient synthesis of L-thioarabinose derivative: A versatile synthon for the synthesis of L-2′-deoxy-2′,2′ -disubstituted-4′-thionucleosides
-
Jeong, L. S.; Moon, H. R.; Choi, Y. J.; Chun, M. W.; Kim, H. O. A short and efficient synthesis of L-thioarabinose derivative: a versatile synthon for the synthesis of L-2′-deoxy-2′,2′-disubstituted-4′ -thionucleosides. J. Org. Chem. 1998, 63, 4821-4825.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 4821-4825
-
-
Jeong, L.S.1
Moon, H.R.2
Choi, Y.J.3
Chun, M.W.4
Kim, H.O.5
-
38
-
-
0032563960
-
Synthesis and biological activity of certain 4′ -thio-D-arabinofuranosylpurine nucleosides
-
(a) Secrist, J. A., III; Tiwari, K. N.; Shortnacy-Fowler, A. T.; Messini, L.; Riordan, J. M.; Montgomery, J. A. Synthesis and biological activity of certain 4′-thio-D-arabinofuranosylpurine nucleosides. J. Med. Chem. 1998, 41, 3865-3871.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3865-3871
-
-
Secrist III, J.A.1
Tiwari, K.N.2
Shortnacy-Fowler, A.T.3
Messini, L.4
Riordan, J.M.5
Montgomery, J.A.6
-
39
-
-
0027493548
-
The synthesis and biological of 1-(2′-deoxy-4′-thio-α -L-threo-pentofuranosyl)thymine
-
(b) Tiwari, K.; Montgomery, J. A.; Secrist, J. A., III. The synthesis and biological of 1-(2′-deoxy-4′-thio-α -L-threo-pentofuranosyl)thymine. Nucleosides Nucleotides 1993, 12, 841-846.
-
(1993)
Nucleosides Nucleotides
, vol.12
, pp. 841-846
-
-
Tiwari, K.1
Montgomery, J.A.2
Secrist III, J.A.3
-
40
-
-
0026674841
-
Efficient synthesis of 4-thio-D-ribofuranose and some 4′-thioribonucleosides
-
Bellon, L.; Barascut, J.-L.; Imbach, J.-L. Efficient synthesis of 4-thio-D-ribofuranose and some 4′-thioribonucleosides. Nucleosides Nucleotides 1992, 11, 1467-1479.
-
(1992)
Nucleosides Nucleotides
, vol.11
, pp. 1467-1479
-
-
Bellon, L.1
Barascut, J.-L.2
Imbach, J.-L.3
-
41
-
-
0036498808
-
Efficient synthesis of 2-deoxy-L-erythropentose (2-deoxy-L-ribose) from L-arabinose
-
Chong, Y.; Chu, C. K. Efficient synthesis of 2-deoxy-L-erythropentose (2-deoxy-L-ribose) from L-arabinose. Carbohyd. Res. 2002, 337, 397-402.
-
(2002)
Carbohyd. Res.
, vol.337
, pp. 397-402
-
-
Chong, Y.1
Chu, C.K.2
-
42
-
-
0027409698
-
Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides
-
Schinazi, R. F.; Lloyd, R. M.; Nguyen, M.-N.; Cannon, D. L.; McMillan, A.; Ilksoy, N.; Chu, C. K.; Liotta, D. C.; Bazmi, H. Z.; Mellors, J. W. Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides. Antimicrob. Agents Chemother. 1993, 37, 875-881.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 875-881
-
-
Schinazi, R.F.1
Lloyd, R.M.2
Nguyen, M.-N.3
Cannon, D.L.4
McMillan, A.5
Ilksoy, N.6
Chu, C.K.7
Liotta, D.C.8
Bazmi, H.Z.9
Mellors, J.W.10
-
43
-
-
0003854857
-
-
FDA talk paper available at http://www.fda.gov/bbs/topics/ANSWERS/2001/ANS01111.html.
-
FDA Talk Paper
-
-
-
44
-
-
0032573488
-
Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance
-
Huang, H.; Chopra, R.; Verdine, G. L.; Harrison, S. C. Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance. Science 1998, 282, 1669-1675.
-
(1998)
Science
, vol.282
, pp. 1669-1675
-
-
Huang, H.1
Chopra, R.2
Verdine, G.L.3
Harrison, S.C.4
-
45
-
-
0038240528
-
Molecular mechanism of DAPD/DXG against zidovudine- and lamivudine-drug resistant mutants: A molecular modeling approach
-
(a) Chong, Y.; Borroto-Esoda, K.; Furman, P. A.; Schinazi, R. F.; Chu, C. K. Molecular mechanism of DAPD/DXG against zidovudine- and lamivudine-drug resistant mutants: a molecular modeling approach. Antiviral Chem. Chemother. 2002, 13, 115-128.
-
(2002)
Antiviral Chem. Chemother.
, vol.13
, pp. 115-128
-
-
Chong, Y.1
Borroto-Esoda, K.2
Furman, P.A.3
Schinazi, R.F.4
Chu, C.K.5
-
46
-
-
0035173806
-
Molecular modeling approach to understanding the mode of action of L-nucleosides as antiviral agents
-
(b) Lee, K.; Chu, C. K. Molecular modeling approach to understanding the mode of action of L-nucleosides as antiviral agents. Antimicrob. Agents Chemother. 2001, 45, 138-144.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 138-144
-
-
Lee, K.1
Chu, C.K.2
-
47
-
-
0030937244
-
Organic fluorine hardly ever accepts hydrogen bonds
-
Dunitz, J. D.; Taylor, R. Organic fluorine hardly ever accepts hydrogen bonds. Chem.-Eur. J. 1997, 3, 89-98.
-
(1997)
Chem.-Eur. J.
, vol.3
, pp. 89-98
-
-
Dunitz, J.D.1
Taylor, R.2
-
48
-
-
0028003745
-
Multiple drug effect analysis with confidence interval
-
Belen'kii, S. M.; Schinazi, R. S. Multiple drug effect analysis with confidence interval. Antiviral Res. 1994, 25, 1-11.
-
(1994)
Antiviral Res.
, vol.25
, pp. 1-11
-
-
Belen'kii, S.M.1
Schinazi, R.S.2
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