-
1
-
-
0034839886
-
Synthesis, hydrolysis and anti-EBV activity of a series of 3′-modified cycloSal-BVDUMP pronucleotides
-
Meier, C.; Lomp, A.; Meerbach, A.; Wutzler, P. Synthesis, hydrolysis and anti-EBV activity of a series of 3′-modified cycloSal-BVDUMP pronucleotides. Nucleosides Nucleotides 2001, 20, 307-314.
-
(2001)
Nucleosides Nucleotides
, vol.20
, pp. 307-314
-
-
Meier, C.1
Lomp, A.2
Meerbach, A.3
Wutzler, P.4
-
2
-
-
0033826441
-
Novel approaches for designing 5′-O-ester prodrugs of 3′-azido-2′,3′-dideoxythymidine (AZT)
-
Parang, K.; Wiebe, L. I.; Knaus, E. E. Novel Approaches for Designing 5′-O-Ester Prodrugs of 3′-Azido-2′,3′-dideoxythymidine (AZT). Curr. Med. Chem. 2000, 7, 995-1039.
-
(2000)
Curr. Med. Chem.
, vol.7
, pp. 995-1039
-
-
Parang, K.1
Wiebe, L.I.2
Knaus, E.E.3
-
4
-
-
0033736202
-
Pronucleotides: Towards the in vivo delivery of antiviral and anticancer nucleotides
-
Wagner, C. R.; Iyer, V. V.; McIntee, E. J. Pronucleotides: Towards the in vivo delivery of antiviral and anticancer nucleotides. Med. Res. Rev. 2000, 20, 417-451.
-
(2000)
Med. Res. Rev.
, vol.20
, pp. 417-451
-
-
Wagner, C.R.1
Iyer, V.V.2
McIntee, E.J.3
-
5
-
-
0034676311
-
S-acyl-2-thioethyl aryl phosphotriester derivatives as mononucleotide prodrugs
-
Schlienger, N.; Peyrottes, S.; Kassem, T.; Imbach, J.-L.; Gosselin, G.; et al. S-Acyl-2-thioethyl Aryl Phosphotriester Derivatives as Mononucleotide Prodrugs. J. Med. Chem. 2000, 43, 4570-4574.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4570-4574
-
-
Schlienger, N.1
Peyrottes, S.2
Kassem, T.3
Imbach, J.-L.4
Gosselin, G.5
-
6
-
-
0006202716
-
New methods and reagents in organic synthesis 67. A general synthesis of derivatives of optically pure 2-(1-aminoalkyl)-thiazole-4-carboxylic acids
-
Hamada, Y.; Shibata, M.; Sugiura, T.; Kato, S.; Shiori, T. New methods and reagents in organic synthesis. 67. A general synthesis of derivatives of optically pure 2-(1-aminoalkyl)-thiazole-4-carboxylic acids. J. Org. Chem. 1987, 52, 1252-1255.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 1252-1255
-
-
Hamada, Y.1
Shibata, M.2
Sugiura, T.3
Kato, S.4
Shiori, T.5
-
7
-
-
33748902391
-
The total synthesis of the diepoxycyclohexanone antibiotic aranorosin and novel synthetic analogues
-
McKillop, A.; McLaren, L.; Taylor, R. J. K.; Watson, R. J.; Lewis, N. J. The total synthesis of the diepoxycyclohexanone antibiotic aranorosin and novel synthetic analogues. J. Chem. Soc., Perkin Trans. 1 1996, 1385-1393.
-
(1996)
J. Chem. Soc., Perkin Trans. 1
, pp. 1385-1393
-
-
McKillop, A.1
McLaren, L.2
Taylor, R.J.K.3
Watson, R.J.4
Lewis, N.J.5
-
8
-
-
0026443973
-
Synthesis of (S,S)-isodityrosinol in a fully differentiated form via Diels-Alder methodology
-
Feng, X.; Olsen, R. K. Synthesis of (S,S)-isodityrosinol in a fully differentiated form via Diels-Alder methodology. J. Org. Chem. 1992, 57, 5811-5812.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5811-5812
-
-
Feng, X.1
Olsen, R.K.2
-
9
-
-
0021464714
-
Practical procedure for the chemoselective reduction of esters by sodium borohydride. Effect of the slow addition of methanol
-
Soai, K.; Oyamada, H.; Tanase, M.; Ookawa, A. Practical procedure for the chemoselective reduction of esters by sodium borohydride. Effect of the slow addition of methanol. Bull. Chem. Soc. Jpn. 1984, 57, 1948-1953.
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 1948-1953
-
-
Soai, K.1
Oyamada, H.2
Tanase, M.3
Ookawa, A.4
-
10
-
-
29644432244
-
Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives
-
Corey, E. J.; Venkateswarlu, A. Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives. J. Am. Chem. Soc. 1972, 94, 6190-6191.
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 6190-6191
-
-
Corey, E.J.1
Venkateswarlu, A.2
-
11
-
-
0033588083
-
Photocleavable protecting groups as nucleobase protections allowed the solid-phase synthesis of base-sensitive SATE-prooligonucleotides
-
Alvarez, K.; Vasseur, J.-J.; Beltran, T.; Imbach, J.-L. Photocleavable protecting groups as nucleobase protections allowed the solid-phase synthesis of base-sensitive SATE-prooligonucleotides. J. Org. Chem. 1999, 64, 6319-6328.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 6319-6328
-
-
Alvarez, K.1
Vasseur, J.-J.2
Beltran, T.3
Imbach, J.-L.4
-
12
-
-
0029796002
-
Comparison of cytotoxicity of mononucleoside phosphotriester derivatives bearing biolabile phosphate protecting groups in normal human bone marrow progenitor cells
-
Périgaud, C.; Girardet, J.-L.; Lefebvre, I.; Xie, M.-Y.; Aubertin, A.-M.; et al. Comparison of cytotoxicity of mononucleoside phosphotriester derivatives bearing biolabile phosphate protecting groups in normal human bone marrow progenitor cells. Antiviral Chem. Chemother. 1996, 7, 338-345.
-
(1996)
Antiviral Chem. Chemother.
, vol.7
, pp. 338-345
-
-
Périgaud, C.1
Girardet, J.-L.2
Lefebvre, I.3
Xie, M.-Y.4
Aubertin, A.-M.5
-
13
-
-
0032731244
-
Intracellular metabolism of CycloSaligenyl 3′-azido-2′,3′-dideoxythymidine monophosphate, a prodrug of 3′-azido-2′,3′-dideoxythymidine (Zidovudine)
-
Balzarini, J.; Naesens, L.; Aquaro, S.; Knispel, T.; Perno, C.; et al. Intracellular metabolism of CycloSaligenyl 3′-azido-2′,3′-dideoxythymidine monophosphate, a prodrug of 3′-azido-2′,3′-dideoxythymidine (Zidovudine). Mol. Pharmacol. 1999, 6, 1354-1361.
-
(1999)
Mol. Pharmacol.
, vol.6
, pp. 1354-1361
-
-
Balzarini, J.1
Naesens, L.2
Aquaro, S.3
Knispel, T.4
Perno, C.5
-
14
-
-
0028819889
-
Mononucleoside phosphotriester derivatives with S-acyl-2-thioethyl bioreversible phosphate protecting groups. Intracellular delivery of 3′-azido-2′,3′-dideoxythymidine 5′-monophosphate
-
Lefebvre, I.; Périgaud, C.; Pompon, A.; Aubertin, A.-M.; Girardet, J.-L.; et al. Mononucleoside phosphotriester derivatives with S-acyl-2-thioethyl bioreversible phosphate protecting groups. Intracellular delivery of 3′-azido-2′,3′-dideoxythymidine 5′-monophosphate. J. Med. Chem. 1995, 38, 3941-3950.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3941-3950
-
-
Lefebvre, I.1
Périgaud, C.2
Pompon, A.3
Aubertin, A.-M.4
Girardet, J.-L.5
-
15
-
-
0027501126
-
5′-hydrogenphosphonates of anti-HIV nucleoside analogues revisited: Controversial mode of action
-
Gosselin, G.; Périgaud, C.; Lefebvre, I.; Pompon, A.; Aubertin, A.-M.; et al. 5′-Hydrogenphosphonates of anti-HIV nucleoside analogues revisited: Controversial mode of action. Antiviral Res. 1993, 22, 143-153.
-
(1993)
Antiviral Res.
, vol.22
, pp. 143-153
-
-
Gosselin, G.1
Périgaud, C.2
Lefebvre, I.3
Pompon, A.4
Aubertin, A.-M.5
-
16
-
-
0023664002
-
A model study directed towards the preparation of nucleopeptides via H-phosphonate intermediates
-
Kuyl-Yeheskiely, E.; Tromp, C. M.; Schaeffer, A. H.; Vander Marel, G. A.; Van Boom, J. H. A model study directed towards the preparation of nucleopeptides via H-phosphonate intermediates. Nucleic Acids Res. 1987, 15, 1807-1818.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 1807-1818
-
-
Kuyl-Yeheskiely, E.1
Tromp, C.M.2
Schaeffer, A.H.3
Vander Marel, G.A.4
Van Boom, J.H.5
-
17
-
-
0030803864
-
Aryl H-phosphonates. 6. Synthetic studies on the preparation of nucleosides N-alkyl-H-phosphonamidates
-
Sobkowska, A.; Sobkowski, M.; Cieslak, J.; Kraszewski, A. Aryl H-phosphonates. 6. Synthetic studies on the preparation of nucleosides N-alkyl-H-phosphonamidates. J. Org. Chem. 1997, 62, 4791-4794.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4791-4794
-
-
Sobkowska, A.1
Sobkowski, M.2
Cieslak, J.3
Kraszewski, A.4
-
18
-
-
0034846309
-
Design of new mononucleotide prodrugs: Aryl (SATE) phosphotriester derivatives
-
Peyrottes, S.; Schlienger, N.; Beltran, T.; Lefebvre, I.; Pompon, A.; et al. Design of new mononucleotide prodrugs: Aryl (SATE) phosphotriester derivatives. Nucleosides Nucleotides 2001, 20, 315-321.
-
(2001)
Nucleosides Nucleotides
, vol.20
, pp. 315-321
-
-
Peyrottes, S.1
Schlienger, N.2
Beltran, T.3
Lefebvre, I.4
Pompon, A.5
-
19
-
-
78651147451
-
Reactions catalyzed by amidases
-
Jakoby, W. B.; Fredericks, J. Reactions catalyzed by amidases. J. Biol. Chem. 1964, 239, 1978-1982.
-
(1964)
J. Biol. Chem.
, vol.239
, pp. 1978-1982
-
-
Jakoby, W.B.1
Fredericks, J.2
-
20
-
-
0025103948
-
Selective deamidation of peptide amides
-
Steinke, D.; Kula, M. R. Selective deamidation of peptide amides. Angew. Chem., Int. Ed. Engl. 1990, 29, 1139-1140.
-
(1990)
Angew. Chem., Int. Ed. Engl.
, vol.29
, pp. 1139-1140
-
-
Steinke, D.1
Kula, M.R.2
-
21
-
-
0031731022
-
The catalytic mechanism of amidase also involves nitrile hydrolysis
-
Kobayashi, M.; Goda, M.; Shimizu, S. The catalytic mechanism of amidase also involves nitrile hydrolysis. FEBS Lett. 1998, 439, 325-328.
-
(1998)
FEBS Lett.
, vol.439
, pp. 325-328
-
-
Kobayashi, M.1
Goda, M.2
Shimizu, S.3
-
22
-
-
0033110788
-
Isolation and primary characterization of an amidase from Rhodococcus rhodochrous
-
Kotlova, E.; Chestukhina, G.; Astaurova, O.; Leonova, T.; Yanenko, A.; et al. Isolation and primary characterization of an amidase from Rhodococcus rhodochrous. Biochemistry 1999, 64, 384-389.
-
(1999)
Biochemistry
, vol.64
, pp. 384-389
-
-
Kotlova, E.1
Chestukhina, G.2
Astaurova, O.3
Leonova, T.4
Yanenko, A.5
-
23
-
-
0029996889
-
Purification and properties of an amidase from Rhodococcus erythropolis MP50 which enantioselectively hydrolyzes 2-arylpropionamides
-
Hirrlinger, B.; Stolz, A.; Knackmuss, H. J. Purification and properties of an amidase from Rhodococcus erythropolis MP50 which enantioselectively hydrolyzes 2-arylpropionamides. J. Bacteriol. 1996, 178, 3501-3507.
-
(1996)
J. Bacteriol.
, vol.178
, pp. 3501-3507
-
-
Hirrlinger, B.1
Stolz, A.2
Knackmuss, H.J.3
-
24
-
-
0027488920
-
Amidase coupled with low-molecular-mass nitrile hydratase from Rhodococcus rhodochrous J1
-
Kobayashi, M.; Komeda, H.; Nagasawa, T.; Nishiyama, M.; Horinouchi, S.; et al. Amidase coupled with low-molecular-mass nitrile hydratase from Rhodococcus rhodochrous J1. Eur. J. Biochem. 1993, 217, 327-336.
-
(1993)
Eur. J. Biochem.
, vol.217
, pp. 327-336
-
-
Kobayashi, M.1
Komeda, H.2
Nagasawa, T.3
Nishiyama, M.4
Horinouchi, S.5
-
25
-
-
0001741836
-
The aliphatic amidases Pseudomonas aeruginosa
-
Academic Press: London
-
Clarke, P. H. The aliphatic amidases Pseudomonas aeruginosa. Advances in Microbial Physiology; Academic Press: London, 1970; pp 179-222.
-
(1970)
Advances in Microbial Physiology
, pp. 179-222
-
-
Clarke, P.H.1
-
26
-
-
0016747613
-
Hydrolysis of phosphate esters catalyzed by 5′-nucleotide phosphodiesterase
-
Kelly, S. J.; Dardinger, D. E.; Butler, L. G. Hydrolysis of phosphate esters catalyzed by 5′-nucleotide phosphodiesterase. Biochemistry 1975, 14, 4983-4988.
-
(1975)
Biochemistry
, vol.14
, pp. 4983-4988
-
-
Kelly, S.J.1
Dardinger, D.E.2
Butler, L.G.3
-
27
-
-
0001646976
-
Synthesis and studies of mononucleoside glucosyl phosphotriester derivatives
-
Schlienger, N.; Périgaud, C.; Gosselin, G.; Imbach, J.-L. Synthesis and studies of mononucleoside glucosyl phosphotriester derivatives. J. Org. Chem. 1997, 62, 7216-7221.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7216-7221
-
-
Schlienger, N.1
Périgaud, C.2
Gosselin, G.3
Imbach, J.-L.4
-
28
-
-
0025924002
-
A rapid microscale method for the determination of partition coefficients by HPLC
-
Ford, H., Jr.; Merski, C. L.; Kelley, J. A. A rapid microscale method for the determination of partition coefficients by HPLC. J. Liq. Chromatogr. 1991, 14, 3365-3386.
-
(1991)
J. Liq. Chromatogr.
, vol.14
, pp. 3365-3386
-
-
Ford H., Jr.1
Merski, C.L.2
Kelley, J.A.3
-
29
-
-
37049098563
-
Formation of by-products during sodium-liquid ammonia reduction in peptide chemistry
-
Schön, I.; Szirts, T.; Uberhadt, T. Formation of by-products during sodium-liquid ammonia reduction in peptide chemistry. J. Chem. Soc., Chem. Commun. 1982, 11, 639-640.
-
(1982)
J. Chem. Soc., Chem. Commun.
, vol.11
, pp. 639-640
-
-
Schön, I.1
Szirts, T.2
Uberhadt, T.3
|