-
1
-
-
0018968225
-
Alkylating nucleosides. 5. Synthesis and cytostatic activity of N-ribosyl-halomethyl-1,2,3-triazoles
-
Alonso R, Camarasa MJ, Alonso G & De las Heras FG (1980) Alkylating nucleosides. 5. Synthesis and cytostatic activity of N-ribosyl-halomethyl-1,2,3-triazoles. European Journal of Medicinal Chemistry 15:105-109.
-
(1980)
European Journal of Medicinal Chemistry
, vol.15
, pp. 105-109
-
-
Alonso, R.1
Camarasa, M.J.2
Alonso, G.3
De Las Heras, F.G.4
-
2
-
-
0030785190
-
Synthesis and anti-human immunodeficiency virus type 1 activity of novel 3′-spiro nucleoside analogues of TSAO-T
-
Alvarez R, Jimeno ML, Pérez-Pérez MJ, De Clercq E, Balzarini J & Camarasa MJ (1997) Synthesis and anti-human immunodeficiency virus type 1 activity of novel 3′-spiro nucleoside analogues of TSAO-T. Antiviral Chemistry & Chemotherapy 8:507-509.
-
(1997)
Antiviral Chemistry & Chemotherapy
, vol.8
, pp. 507-509
-
-
Alvarez, R.1
Jimeno, M.L.2
Pérez-Pérez, M.J.3
De Clercq, E.4
Balzarini, J.5
Camarasa, M.J.6
-
3
-
-
0031818269
-
Novel 3′-spiro nucleoside analogues of TSAO-T. Part II. A comparative study based on NMR conformational analysis in solution and theoretical calculations
-
Alvarez R, Jimeno ML, Gago F, Balzarini J, Pérez-Pérez MJ & Camarasa MJ (1998) Novel 3′-spiro nucleoside analogues of TSAO-T. Part II. A comparative study based on NMR conformational analysis in solution and theoretical calculations. Antiviral Chemistry & Chemotherapy 9:123-133.
-
(1998)
Antiviral Chemistry & Chemotherapy
, vol.9
, pp. 123-133
-
-
Alvarez, R.1
Jimeno, M.L.2
Gago, F.3
Balzarini, J.4
Pérez-Pérez, M.J.5
Camarasa, M.J.6
-
4
-
-
0028063421
-
1,2,3-Triazole-[2′,5′-bis-O-tert-butyldimethylsilyl-β-D- ribofuranosyl]-3′-spiro-5″-(4″-amino-1″,2″- oxathiole-2″,2″-dioxide) (TSAO) analogues. Synthesis and anti-HIV-1 activity
-
Alvarez R, Velázquez S, San-Félix A, Aquaro S, De Clercq E, Perno C-F, Karlsson A, Balzarini J & Camarasa MJ (1994) 1,2,3-Triazole-[2′,5′-bis-O-tert-butyldimethylsilyl-β-D- ribofuranosyl]-3′-spiro-5″-(4″-amino-1″,2″- oxathiole-2″,2″-dioxide) (TSAO) analogues. Synthesis and anti-HIV-1 activity. Journal of Medicinal Chemistry 37:4185-4194.
-
(1994)
Journal of Medicinal Chemistry
, vol.37
, pp. 4185-4194
-
-
Alvarez, R.1
Velázquez, S.2
San-Félix, A.3
Aquaro, S.4
De Clercq, E.5
Perno, C.-F.6
Karlsson, A.7
Balzarini, J.8
Camarasa, M.J.9
-
5
-
-
0026724892
-
Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1 specific nucleoside analogue 2′,5′-bis-O-(t-butyldimethylsilyl)-3′-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide) thymine (TSAO-T)
-
Balzarini J, Pérez-Pérez MJ, San-Félix A, Camarasa MJ, Bathurst IC, Barr PJ & De Clercq E (1992a) Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1 specific nucleoside analogue 2′,5′-bis-O-(t-butyldimethylsilyl)-3′-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide) thymine (TSAO-T). Journal of Biological Chemistry 267:11831-11838.
-
(1992)
Journal of Biological Chemistry
, vol.267
, pp. 11831-11838
-
-
Balzarini, J.1
Pérez-Pérez, M.J.2
San-Félix, A.3
Camarasa, M.J.4
Bathurst, I.C.5
Barr, P.J.6
De Clercq, E.7
-
6
-
-
0026606044
-
2′,5′-Bis-O-(tert-butyldimethylsilyl)-3′-spiro- 5″-(4″-amino-1″,2″-oxathiole-2″,2″-dioxide) pyrimidine (TSAO) nucleoside analogues: Highly selective inhibitors of human immunodeficiency virus type 1 that are targeted at the viral reverse transcriptase
-
Balzarini J, Pérez-Pérez MJ, San-Félix A, Schols D, Perno CF, Vandamme AM, Camarasa MJ & De Clercq E (1992b) 2′,5′-Bis-O-(tert-butyldimethylsilyl)-3′-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide)pyrimidine (TSAO) nucleoside analogues: highly selective inhibitors of human immunodeficiency virus type 1 that are targeted at the viral reverse transcriptase. Proceedings of the National Academy of Sciences, USA 89:4392-4396.
-
(1992)
Proceedings of the National Academy of Sciences, USA
, vol.89
, pp. 4392-4396
-
-
Balzarini, J.1
Pérez-Pérez, M.J.2
San-Félix, A.3
Schols, D.4
Perno, C.F.5
Vandamme, A.M.6
Camarasa, M.J.7
De Clercq, E.8
-
7
-
-
0026694001
-
[2′,5′-Bis-O-tert-butyldimethylsilyl]-3′-spiro- 5″-(4″-amino-1″,2″-oxathiole-2″,2″-dioxide) (TSAO) derivatives of purine and pyrimidine nucleosides as potent and selective inhibitors of human immunodeficiency virus type 1
-
Balzarini J, Pérez-Pérez MJ, San-Félix A, Velázquez S, Camarasa MJ & De Clercq E (1992c) [2′,5′-Bis-O-tert-butyldimethylsilyl)]-3′-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide) (TSAO) derivatives of purine and pyrimidine nucleosides as potent and selective inhibitors of human immunodeficiency virus type 1. Antimicrobial Agents and Chemotherapy 36:1073-1080.
-
(1992)
Antimicrobial Agents and Chemotherapy
, vol.36
, pp. 1073-1080
-
-
Balzarini, J.1
Pérez-Pérez, M.J.2
San-Félix, A.3
Velázquez, S.4
Camarasa, M.J.5
De Clercq, E.6
-
8
-
-
0027328082
-
HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1 mutant strains containing different ammo acid substitutions in the reverse transcriptase
-
Balzarini J, Karlsson A, Pérez-Pérez MJ, Vrang L, Walbers J, Zhang H, Öberg B, Vandamme AM, Camarasa MJ & De Clercq E (1993a) HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1 mutant strains containing different ammo acid substitutions in the reverse transcriptase. Virology 192:246-253.
-
(1993)
Virology
, vol.192
, pp. 246-253
-
-
Balzarini, J.1
Karlsson, A.2
Pérez-Pérez, M.J.3
Vrang, L.4
Walbers, J.5
Zhang, H.6
Öberg, B.7
Vandamme, A.M.8
Camarasa, M.J.9
De Clercq, E.10
-
9
-
-
0027763366
-
TSAO derivatives: Highly specific human immunodeficiency virus type 1 (HIV-1) reverse transcriptase inhibitors
-
Balzarini J, Camarasa MJ & Karlsson A (1993b) TSAO derivatives: Highly specific human immunodeficiency virus type 1 (HIV-1) reverse transcriptase inhibitors. Drugs of the Future 18:1043-1055.
-
(1993)
Drugs of the Future
, vol.18
, pp. 1043-1055
-
-
Balzarini, J.1
Camarasa, M.J.2
Karlsson, A.3
-
10
-
-
0028068907
-
Sensitivity of (138 GLU → LYS) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors
-
Balzarini J, Kleim JP, Riess G, Camarasa MJ, De Clercq E & Karlsson A (1994) Sensitivity of (138 GLU → LYS) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors. Biochemical and Biophysical Research Communications 201:1305-1312.
-
(1994)
Biochemical and Biophysical Research Communications
, vol.201
, pp. 1305-1312
-
-
Balzarini, J.1
Kleim, J.P.2
Riess, G.3
Camarasa, M.J.4
De Clercq, E.5
Karlsson, A.6
-
13
-
-
0028024028
-
Subunit specificity of mutations that confer resistance to nonnucleoside inhibitors in human immunodeficiency virus type 1 reverse transcriptase
-
Boyer PL, Ding J, Arnold E & Hughes SH (1994) Subunit specificity of mutations that confer resistance to nonnucleoside inhibitors in human immunodeficiency virus type 1 reverse transcriptase. Antimicrobial Agents and Chemotherapy 38:1909-1914.
-
(1994)
Antimicrobial Agents and Chemotherapy
, vol.38
, pp. 1909-1914
-
-
Boyer, P.L.1
Ding, J.2
Arnold, E.3
Hughes, S.H.4
-
14
-
-
0026771409
-
3́-Spironucleosides (TSAO derivatives), a new class of specific human immunodeficiency virus type 1 inhibitors: Synthesis and antiviral activity of 3′-spiro-5″-[4″-amino-1″,2″-oxathiole-2″, 2″-dioxide]pyrimidine nucleosides
-
Camarasa MJ, Pérez-Pérez MJ, San-Félix A, Balzarini J & De Clercq E (1992) 3́-Spironucleosides (TSAO derivatives), a new class of specific human immunodeficiency virus type 1 inhibitors: synthesis and antiviral activity of 3′-spiro-5″-[4″-amino-1″,2″-oxathiole-2″, 2″-dioxide]pyrimidine nucleosides. Journal of Medicinal Chemistry 35:2721-12727.
-
(1992)
Journal of Medicinal Chemistry
, vol.35
, pp. 2721-12727
-
-
Camarasa, M.J.1
Pérez-Pérez, M.J.2
San-Félix, A.3
Balzarini, J.4
De Clercq, E.5
-
15
-
-
0029036852
-
TSAO derivatives: Highly specific inhibitors of human immunodeficiency virus type-1 (HIV-1) replication
-
Camarasa MJ, Pérez-Pérez MJ, Velázquez S, San-Félix A, Alvarez A, Ingate S, Jimeno ML, Karlsson A, De Clercq E & Balzarini J (1995) TSAO derivatives: highly specific inhibitors of human immunodeficiency virus type-1 (HIV-1) replication. Nucleosides and Nucleotides 14:585-594.
-
(1995)
Nucleosides and Nucleotides
, vol.14
, pp. 585-594
-
-
Camarasa, M.J.1
Pérez-Pérez, M.J.2
Velázquez, S.3
San-Félix, A.4
Alvarez, A.5
Ingate, S.6
Jimeno, M.L.7
Karlsson, A.8
De Clercq, E.9
Balzarini, J.10
-
16
-
-
0027447133
-
HIV-1 specific RT inhibitors: Highly selective inhibitors of human immunodeficiency virus type 1 that are specifically targeted at the viral reverse transcriptase
-
De Clercq E (1993) HIV-1 specific RT inhibitors: highly selective inhibitors of human immunodeficiency virus type 1 that are specifically targeted at the viral reverse transcriptase. Medicinal Research Reviews 13:229-258.
-
(1993)
Medicinal Research Reviews
, vol.13
, pp. 229-258
-
-
De Clercq, E.1
-
17
-
-
0029011730
-
Towards improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
-
De Clercq E (1995) Towards improved anti-HIV chemotherapy: therapeutic strategies for intervention with HIV infections. Journal of Medicinal Chemistry 38:2491-2517.
-
(1995)
Journal of Medicinal Chemistry
, vol.38
, pp. 2491-2517
-
-
De Clercq, E.1
-
18
-
-
0029877789
-
Nonnucleoside reverse transcriptase inhibitors (NNRTIs) for the treatment of human immunodeficiency virus type 1 (HIV-1) infections: Strategies to overcome drug resistance development
-
De Clercq E (1996) Nonnucleoside reverse transcriptase inhibitors (NNRTIs) for the treatment of human immunodeficiency virus type 1 (HIV-1) infections: strategies to overcome drug resistance development. Medicinal Research Reviews 16:125-157.
-
(1996)
Medicinal Research Reviews
, vol.16
, pp. 125-157
-
-
De Clercq, E.1
-
20
-
-
0030935265
-
Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis(heteroaryl)piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitor
-
Esnouf RM, Ren J, Hopkins AL, Ross CK, Jones EY, Stammers DK & Stuart DI (1997) Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis(heteroaryl)piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitor. Proceedings of the National Academy of Sciences, USA 94:3984-3989.
-
(1997)
Proceedings of the National Academy of Sciences, USA
, vol.94
, pp. 3984-3989
-
-
Esnouf, R.M.1
Ren, J.2
Hopkins, A.L.3
Ross, C.K.4
Jones, E.Y.5
Stammers, D.K.6
Stuart, D.I.7
-
22
-
-
0021871375
-
A computational procedure for determining energetically favorable binding sites on biologically important macromolecules
-
Goodford PJ (1985) A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. Journal of Medicinal Chemistry 28:849-857.
-
(1985)
Journal of Medicinal Chemistry
, vol.28
, pp. 849-857
-
-
Goodford, P.J.1
-
25
-
-
0001537783
-
The reactions of phosphorous compounds. XII. A new synthesis of 1,2,3-triazoles and diazo esters from phosphorous ylids and azides
-
Harvey GR (1966) The reactions of phosphorous compounds. XII. A new synthesis of 1,2,3-triazoles and diazo esters from phosphorous ylids and azides. Journal of Organic Chemistry 31:1587-1590.
-
(1966)
Journal of Organic Chemistry
, vol.31
, pp. 1587-1590
-
-
Harvey, G.R.1
-
27
-
-
0027318776
-
Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 Å resolution shows bent DNA
-
Jacobo-Molina A, Ding J, Nanni RG, Clark AD Jr, Lu X, Tantillo C, Williams RL, Kamer G, Ferris AL, Clark P, Hizi A, Hughes SH & Arnold E (1993) Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 Å resolution shows bent DNA. Proceedings of the National Academy of Sciences, USA 90:6320-6324.
-
(1993)
Proceedings of the National Academy of Sciences, USA
, vol.90
, pp. 6320-6324
-
-
Jacobo-Molina, A.1
Ding, J.2
Nanni, R.G.3
Clark Jr., A.D.4
Lu, X.5
Tantillo, C.6
Williams, R.L.7
Kamer, G.8
Ferris, A.L.9
Clark, P.10
Hizi, A.11
Hughes, S.H.12
Arnold, E.13
-
28
-
-
0028099251
-
138 → Lys on the p51 subunit
-
138 → Lys on the p51 subunit. Journal of Biological Chemistry 269:25255-25258.
-
(1994)
Journal of Biological Chemistry
, vol.269
, pp. 25255-25258
-
-
Jonckheere, H.1
Taymans, J.M.2
Balzarini, J.3
Velázquez, S.4
Camarasa, M.J.5
Desmyter, J.6
De Clercq, E.7
Anné, J.8
-
30
-
-
84982451578
-
Stereochemistry XLIV. Regiochemistry in cycloaddition reactions of vinylazides with phenylacetylene
-
L'abbé G & Hassner A (1971) Stereochemistry XLIV. Regiochemistry in cycloaddition reactions of vinylazides with phenylacetylene. Bulletin des Societes Chimiques Belges 80:209-210.
-
(1971)
Bulletin des Societes Chimiques Belges
, vol.80
, pp. 209-210
-
-
L'abbé, G.1
Hassner, A.2
-
31
-
-
84918046148
-
Nouvelle voie d'accès aux esters α-cétoniques β-éthyléniques
-
Le Corre M (1970) Nouvelle voie d'accès aux esters α-cétoniques β-éthyléniques. Comptes Rendus de L'Academie des Sciences Serie C 270:1312-11314.
-
(1970)
Comptes Rendus de L'Academie des Sciences Serie C
, vol.270
, pp. 1312-11314
-
-
Le Corre, M.1
-
33
-
-
34250082672
-
Review of HIV-1 reverse transcriptase three-dimensional structure: Implications for drug design
-
Nanni RG, Ding J, Jacobo-Molina A, Hughes SH & Arnold E (1993) Review of HIV-1 reverse transcriptase three-dimensional structure: implications for drug design. Perspectives in Drug Discovery and Design 1:129-1150.
-
(1993)
Perspectives in Drug Discovery and Design
, vol.1
, pp. 129-1150
-
-
Nanni, R.G.1
Ding, J.2
Jacobo-Molina, A.3
Hughes, S.H.4
Arnold, E.5
-
34
-
-
0026737678
-
TSAO-analogues. Stereospecific synthesis and anti-HIV-1 activity of 1-[2′,5′-Bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide) pyrimidine and pyrimidine-modified nucleosides
-
Pérez-Pérez MJ, San-Félix A, Balzarini J, De Clercq E & Camarasa MJ (1992) TSAO-analogues. Stereospecific synthesis and anti-HIV-1 activity of 1-[2′,5′-Bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]- 3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide) pyrimidine and pyrimidine-modified nucleosides. Journal of Medicinal Chemistry 35:2988-2995.
-
(1992)
Journal of Medicinal Chemistry
, vol.35
, pp. 2988-2995
-
-
Pérez-Pérez, M.J.1
San-Félix, A.2
Balzarini, J.3
De Clercq, E.4
Camarasa, M.J.5
-
35
-
-
0028947588
-
High resolution structure of HIV-1 RT: Insights from four RT-inhibitor complexes
-
Ren JS, Esnouf R, Garman E, Jones Y, Somers D, Ross C, Kirby I, Keeling J, Darby G, Stuart D & Stammers D (1995) High resolution structure of HIV-1 RT: insights from four RT-inhibitor complexes. Nature Structural Biology 2:293-302.
-
(1995)
Nature Structural Biology
, vol.2
, pp. 293-302
-
-
Ren, J.S.1
Esnouf, R.2
Garman, E.3
Jones, Y.4
Somers, D.5
Ross, C.6
Kirby, I.7
Keeling, J.8
Darby, G.9
Stuart, D.10
Stammers, D.11
-
36
-
-
85040206888
-
Glycosylazide als Ausgangsbasis zur Gewinnung von Nucleosidanalogen
-
Schörkuber W & Zbiral E (1980) Glycosylazide als Ausgangsbasis zur Gewinnung von Nucleosidanalogen. Liebigs Annalen 1455-1469.
-
(1980)
Liebigs Annalen
, pp. 1455-1469
-
-
Schörkuber, W.1
Zbiral, E.2
-
37
-
-
84982076425
-
Zur synthese von 5-(x-methyl)ribofuranosyl-1,2,3-triazol-nucleosides
-
Schörkuber W & Zbiral E (1981) Zur synthese von 5-(x-methyl)ribofuranosyl-1,2,3-triazol-nucleosides. Chemische Berichte 114:3165-3169.
-
(1981)
Chemische Berichte
, vol.114
, pp. 3165-3169
-
-
Schörkuber, W.1
Zbiral, E.2
-
38
-
-
0028271687
-
Structure of the binding site for non-nucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1
-
USA
-
Smerdon SJ, Jäger J, Wang J, Kohlstaedt LA, Chirino AJ, Friedman JM, Rice PA & Steitz TA (1994) Structure of the binding site for non-nucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1. Proceedings of the National Academy of Sciences, USA 91:3911-3915.
-
(1994)
Proceedings of the National Academy of Sciences
, vol.91
, pp. 3911-3915
-
-
Smerdon, S.J.1
Jäger, J.2
Wang, J.3
Kohlstaedt, L.A.4
Chirino, A.J.5
Friedman, J.M.6
Rice, P.A.7
Steitz, T.A.8
-
39
-
-
0000804347
-
Competitive inhibitors of human immunodeficiency virus reverse transcriptase
-
Schinazi RF (1993) Competitive inhibitors of human immunodeficiency virus reverse transcriptase. Perspectives in Drug Discovery and Design 1:151-180.
-
(1993)
Perspectives in Drug Discovery and Design
, vol.1
, pp. 151-180
-
-
Schinazi, R.F.1
-
41
-
-
0028172345
-
Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance
-
Tantillo C, Ding J, Jacobo-Molina A, Nanni RG, Boyer PL, Hughes SH, Pauwels R, Andries K, Janssen PAJ & Arnold E (1994) Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance. Journal of Molecular Biology 243:369-387.
-
(1994)
Journal of Molecular Biology
, vol.243
, pp. 369-387
-
-
Tantillo, C.1
Ding, J.2
Jacobo-Molina, A.3
Nanni, R.G.4
Boyer, P.L.5
Hughes, S.H.6
Pauwels, R.7
Andries, K.8
Janssen, P.A.J.9
Arnold, E.10
-
42
-
-
34250073329
-
Nonnucleoside inhibitors of HIV-1 reverse transcriptase
-
Young S D (1993) Nonnucleoside inhibitors of HIV-1 reverse transcriptase. Perspectives in Drug Discovery and Design 1:181-192.
-
(1993)
Perspectives in Drug Discovery and Design
, vol.1
, pp. 181-192
-
-
Young, S.D.1
-
44
-
-
15644382546
-
Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse tanscriptase
-
Velázquez S, Chamorro C, Pérez-Pérez MJ, Alvarez R, Jimeno ML, Martín-Domenech A, Pérez C, Gago F, De Clercq E, Balzarini J, San-Félix A & Camarasa MJ (1998) Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse tanscriptase. Journal of Medicinal Chemistry 41:4636-4647
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, pp. 4636-4647
-
-
Velázquez, S.1
Chamorro, C.2
Pérez-Pérez, M.J.3
Alvarez, R.4
Jimeno, M.L.5
Martín-Domenech, A.6
Pérez, C.7
Gago, F.8
De Clercq, E.9
Balzarini, J.10
San-Félix, A.11
Camarasa, M.J.12
-
45
-
-
0028111679
-
Synthesis of [1-[3′,5′-bis-O-tert-butyldimethylsilyl-β-D-arabino-and ribofuranosyl]cytosine]-2′-spiro-5″-(4″-amino-1″, 2″-oxathiole-2″,2″-dioxide). Analogues of the highly specific anti-HIV-1 agent TSAO-T
-
Velázquez S, Jimeno ML, Camarasa MJ & Balzarini J (1994) Synthesis of [1-[3′,5′-bis-O-tert-butyldimethylsilyl-β-D-arabino-and ribofuranosyl]cytosine]-2′-spiro-5″-(4″-amino-1″, 2″-oxathiole-2″,2″-dioxide). Analogues of the highly specific anti-HIV-1 agent TSAO-T. Tetrahedron 50:11013-11022.
-
(1994)
Tetrahedron
, vol.50
, pp. 11013-11022
-
-
Velázquez, S.1
Jimeno, M.L.2
Camarasa, M.J.3
Balzarini, J.4
-
46
-
-
0027437717
-
TSAO analogues. 3. Synthesis and anti-HIV-1 activity of [2′,5′-bis-O-tert-butyldimethylsilyl-β-D-ribofuranosyl]- 3′-spiro-5″-[4″-amino-1″,2″-oxathiole-2″, 2″-dioxide] purine and purine-modified nucleosides
-
Velázquez S, San-Félix A, Pérez-Pérez MJ, Balzarini J, De Clercq E &. Camarasa MJ (1993) TSAO analogues. 3. Synthesis and anti-HIV-1 activity of [2′,5′-bis-O-tert-butyldimethylsilyl-β-D-ribofuranosyl]- 3′-spiro-5″-[4″-amino-1″,2″-oxathiole-2″, 2″-dioxide] purine and purine-modified nucleosides. Journal of Medicinal Chemistry 36:3230-3239.
-
(1993)
Journal of Medicinal Chemistry
, vol.36
, pp. 3230-3239
-
-
Velázquez, S.1
San-Félix, A.2
Pérez-Pérez, M.J.3
Balzarini, J.4
De Clercq, E.5
Camarasa, M.J.6
-
47
-
-
0002965943
-
Synthesen von heterocyclen mit hilfe von alkyliden-phosphoranen phosphin-imiden, vinyl phosphonium-salzen und vinylphosphin-oxiden
-
Zbiral E (1974) Synthesen von heterocyclen mit hilfe von alkyliden-phosphoranen phosphin-imiden, vinyl phosphonium-salzen und vinylphosphin-oxiden. Synthesis 775-800.
-
(1974)
Synthesis
, pp. 775-800
-
-
Zbiral, E.1
|