-
1
-
-
0029154004
-
Synthesis and structure-activity relationships of analogues of 2′-deoxy-2′-(3-methoxybenzamido)adenosine, a selective inhibitor of trypanosomal glycosomal glyceraldehyde-3-phosphate dehydrogenase
-
Van Calenbergh, S.; Verlinde, C. M. L. J.; Soenens, J.; De Bruyn, A.; Callens, M.; Blaton, N. M.; Peeters, O. M.; Rozenski, J.; Hol, W. G.; Herdewijn, P. Synthesis and structure-activity relationships of analogues of 2′-deoxy-2′-(3-methoxybenzamido)adenosine, a selective inhibitor of trypanosomal glycosomal glyceraldehyde-3-phosphate dehydrogenase. J. Med. Chem. 1995, 38, 3838-3849.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3838-3849
-
-
Van Calenbergh, S.1
Verlinde, C.M.L.J.2
Soenens, J.3
De Bruyn, A.4
Callens, M.5
Blaton, N.M.6
Peeters, O.M.7
Rozenski, J.8
Hol, W.G.9
Herdewijn, P.10
-
2
-
-
33748237769
-
Organic chemistry on solid supports
-
Früchtel, J. S.; Jung, G. Organic chemistry on solid supports. Angew. Chem., Int. Ed. 1996, 35, 17-42.
-
(1996)
Angew. Chem., Int. Ed.
, vol.35
, pp. 17-42
-
-
Früchtel, J.S.1
Jung, G.2
-
3
-
-
0032240843
-
Recent advances in solid-phase synthesis
-
Hall, S. Recent advances in solid-phase synthesis. Mol. Diversity 1999, 4, 131-142.
-
(1999)
Mol. Diversity
, vol.4
, pp. 131-142
-
-
Hall, S.1
-
4
-
-
0031603275
-
Recent publications in solid-phase chemistry: Part 2
-
James, I. W. Recent publications in solid-phase chemistry: Part 2. Mol. Diversity 1998, 3, 181-190.
-
(1998)
Mol. Diversity
, vol.3
, pp. 181-190
-
-
James, I.W.1
-
5
-
-
0032497397
-
Combinatorial chemistry: From peptides and peptidomimetics to small organic and heterocyclic compounds
-
Nefzi, A.; Dooley, C. T.; Ostresh, J. M.; Houghten, R. A. Combinatorial chemistry: from peptides and peptidomimetics to small organic and heterocyclic compounds. Bioorg. Med. Chem. Lett. 1998, 8, 2273-2278.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2273-2278
-
-
Nefzi, A.1
Dooley, C.T.2
Ostresh, J.M.3
Houghten, R.A.4
-
6
-
-
0006694681
-
Combinatorial synthesis in medicinal chemistry - Implications in drug discovery
-
Smith, J. R. Combinatorial synthesis in medicinal chemistry -implications in drug discovery. Biomed. Health Res. 1999, 22, 171-177.
-
(1999)
Biomed. Health Res.
, vol.22
, pp. 171-177
-
-
Smith, J.R.1
-
7
-
-
0032879345
-
Phase-trafficking reagents and phase-switching strategies for parallel synthesis
-
Flynn, D. L. Phase-Trafficking Reagents and Phase-Switching Strategies for Parallel Synthesis. Med. Res. Rev. 1999, 19, 409-431.
-
(1999)
Med. Res. Rev.
, vol.19
, pp. 409-431
-
-
Flynn, D.L.1
-
8
-
-
0031741510
-
Polymer-Assisted Solution Phase (PASP) chemical library synthesis
-
Flynn, D. L.; Devraj, R.; Naing, W.; Parlow, J.; Weidner, J.; Yang, S. Polymer-Assisted Solution Phase (PASP) Chemical Library Synthesis. Med. Chem. Res. 1998, 8, 219-243.
-
(1998)
Med. Chem. Res.
, vol.8
, pp. 219-243
-
-
Flynn, D.L.1
Devraj, R.2
Naing, W.3
Parlow, J.4
Weidner, J.5
Yang, S.6
-
9
-
-
0029958205
-
Nucleic acid related compounds. 91. Biomimetic reactions are in harmony with loss of 2′-substituents as free radicals (not anions) during mechanism-based inactivation of ribonucleotide reductases. Differential interactions of Azide, Halogen, and alkylthio groups with tributylstannane and triphenylsilane
-
Robins, M.; Wnuk, S.; Hernández-Thirring, A.; Samano, M. Nucleic Acid Related Compounds. 91. Biomimetic Reactions Are in Harmony with Loss of 2′-Substituents as Free Radicals (Not Anions) during Mechanism-Based Inactivation of Ribonucleotide Reductases. Differential Interactions of Azide, Halogen, and Alkylthio Groups with Tributylstannane and Triphenylsilane. J. Am. Chem. Soc. 1996, 118, 11341-11348.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 11341-11348
-
-
Robins, M.1
Wnuk, S.2
Hernández-Thirring, A.3
Samano, M.4
-
10
-
-
0030007012
-
Synthesis of 2′-amino-2′-deoxyarabino-nucleoside phosphoramidite building blocks
-
Walcher, G.; Pfleiderer, W. Synthesis of 2′-Amino-2′-deoxyarabino-nucleoside Phosphoramidite Building Blocks. Helv. Chim. Acta 1996, 79, 1067-1074.
-
(1996)
Helv. Chim. Acta
, vol.79
, pp. 1067-1074
-
-
Walcher, G.1
Pfleiderer, W.2
-
11
-
-
0000246280
-
Carbon-carbon bond-forming methods on solid support. Utilization of Kenner's "safety-catch" linker
-
Backes, B. J.; Ellman, J. A. Carbon-Carbon Bond-Forming Methods on Solid Support. Utilization of Kenner's "Safety-Catch" Linker. J. Am. Chem. Soc. 1994, 116, 11171-11172.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 11171-11172
-
-
Backes, B.J.1
Ellman, J.A.2
-
12
-
-
0001176887
-
Activation method to prepare a highly reactive acylsulfonamide "safety-catch" linker for solid-phase synthesis
-
Backes, B. J.; Virgilio, A. A.; Ellman, J. A. Activation Method to Prepare a Highly Reactive Acylsulfonamide "Safety-Catch" Linker for Solid-Phase Synthesis. J. Am. Chem. Soc. 1996, 118, 3055-3056.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 3055-3056
-
-
Backes, B.J.1
Virgilio, A.A.2
Ellman, J.A.3
-
13
-
-
0033515621
-
An alkanesulfonamide "safety-catch" linker for solid-phase synthesis
-
Backes, B. J.; Ellman, J. A. An Alkanesulfonamide "Safety-Catch" Linker for Solid-Phase Synthesis. J. Org. Chem. 1999, 64, 2322-2330.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2322-2330
-
-
Backes, B.J.1
Ellman, J.A.2
-
14
-
-
0033584984
-
Solid-phase synthesis of 'head-to-tail' cyclic peptides using a sulfonamide 'safety-catch' linker: The cleavage by cyclization approach
-
Yang, L.; Morriello, G. Solid-phase synthesis of 'head-to-tail' cyclic peptides using a sulfonamide 'safety-catch' linker: the cleavage by cyclization approach. Tetrahedron Lett. 1999, 40, 8197-8200.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 8197-8200
-
-
Yang, L.1
Morriello, G.2
-
15
-
-
0033572729
-
Solid-phase synthesis of peptide C-terminal thioesters by Fmoc/t-Bu chemistry
-
Ingenito, R.; Bianchi, E.; Fattori, D.; Pessi, A. Solid-Phase Synthesis of Peptide C-Terminal Thioesters by Fmoc/t-Bu Chemistry. J. Am. Chem. Soc. 1999, 121, 11369-11374.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 11369-11374
-
-
Ingenito, R.1
Bianchi, E.2
Fattori, D.3
Pessi, A.4
-
16
-
-
0032537689
-
Practical method for the parallel synthesis of 2′-amido-2′-deoxyadenosines
-
Link, A.; van Calenbergh, S.; Herdewijn, P. Practical method for the parallel synthesis of 2′-amido-2′-deoxyadenosines. Tetrahedron Lett. 1998, 39, 5175-5176.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5175-5176
-
-
Link, A.1
Van Calenbergh, S.2
Herdewijn, P.3
-
17
-
-
33751281778
-
A versatile synthon for chemoselective N-acylation reagents, 2-fluoro-N-mesylaniline
-
Kondo, K.; Sekimoto, E.; Miki, K.; Murakami, Y. A versatile synthon for chemoselective N-acylation reagents, 2-fluoro-N-mesylaniline. J. Chem. Soc., Perkin Trans. 1 1998, 2973-2974.
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, vol.1
, pp. 2973-2974
-
-
Kondo, K.1
Sekimoto, E.2
Miki, K.3
Murakami, Y.4
-
18
-
-
0033597843
-
Chiral N-Acyl-tert-butanesulfinamides: The "safety-catch" principle applied to diastereoselective enolate alkylations
-
Backes, B. J.; Dragoli, D. R.; Ellman, J. A. Chiral N-Acyl-tert-butanesulfinamides: The "Safety-Catch" Principle Applied to Diastereoselective Enolate Alkylations. J. Org. Chem. 1999, 64, 5472-5478.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 5472-5478
-
-
Backes, B.J.1
Dragoli, D.R.2
Ellman, J.A.3
-
19
-
-
0032755128
-
Two efficient N-acylation methods mediated by solid-supported reagents for weakly nucleophilic heterocyclic amines
-
Kim, K.; Le, K. Two efficient N-acylation methods mediated by solid-supported reagents for weakly nucleophilic heterocyclic amines. Synlett 1999, 1957-1959.
-
(1999)
Synlett
, pp. 1957-1959
-
-
Kim, K.1
Le, K.2
-
20
-
-
0000482297
-
Solid-supported chloro[1,3,5]triazine. A versatile new synthetic auxiliary for the synthesis of amide libraries
-
Masala, S.; Taddei, M. Solid-Supported Chloro[1,3,5]triazine. A Versatile New Synthetic Auxiliary for the Synthesis of Amide Libraries. Org. Lett. 1999, 1, 1355-1357.
-
(1999)
Org. Lett.
, vol.1
, pp. 1355-1357
-
-
Masala, S.1
Taddei, M.2
-
21
-
-
0034603125
-
Sequential nucleophilic substitution: A powerful strategy for the solid-phase production of diverse compound libraries
-
Zaragoza, F.; Stephensen, H. Sequential Nucleophilic Substitution: A Powerful Strategy for the Solid-Phase Production of Diverse Compound Libraries. Angew. Chem., Int. Ed. 2000, 39, 554-556.
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 554-556
-
-
Zaragoza, F.1
Stephensen, H.2
-
22
-
-
0033214922
-
Liquid-phase synthesis of 2-(alkylthio) benzimidazoles
-
Yeh, C.-M.; Sun, C.-M. Liquid-phase synthesis of 2-(alkylthio) benzimidazoles. Tetrahedron Lett. 1999, 40, 7247-7250.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7247-7250
-
-
Yeh, C.-M.1
Sun, C.-M.2
-
23
-
-
0033551233
-
Structure-based design of submicromolar, biologically active inhibitors of trypanosomatid glyceraldehyde-3-phosphate dehydrogenase
-
Aronov, A. M.; Suresh, S.; Buckner, F. S.; Voorhis, W. C. V.; Verlinde, C. L. M. J.; Opperdoes, F. R.; Hol, W. G. J.; Gelb, M. H. Structure-based design of submicromolar, biologically active inhibitors of trypanosomatid glyceraldehyde-3-phosphate dehydrogenase. Proc. Natl. Acad. Sci. U.S.A. 1999, 96, 4273-4278.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 4273-4278
-
-
Aronov, A.M.1
Suresh, S.2
Buckner, F.S.3
Voorhis, W.C.V.4
Verlinde, C.L.M.J.5
Opperdoes, F.R.6
Hol, W.G.J.7
Gelb, M.H.8
-
24
-
-
0032548073
-
Selective tight binding inhibitors of trypanosomal glyceraldehyde-3-phosphate dehydrogenase via structure-based drug design
-
Aronov, A. M.; Verlinde, C. L. M. J.; Hol, W. G. J.; Gelb, M. H. Selective Tight Binding Inhibitors of Trypanosomal Glyceraldehyde-3-phosphate Dehydrogenase via Structure-Based Drug Design. J. Med. Chem. 1998, 41, 4790-4799.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4790-4799
-
-
Aronov, A.M.1
Verlinde, C.L.M.J.2
Hol, W.G.J.3
Gelb, M.H.4
|