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1
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0028243847
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Applications of combinatorial technologies to drug discovery. I. Background and peptide combinatorial libraries
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For recent reviews see: (a) Gallop, M.A., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gordon, E.M., Applications of combinatorial technologies to drug discovery. I. Background and peptide combinatorial libraries, J. Med. Chem., 37 (1994) 1233-1251.
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Gallop, M.A.1
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Dower, W.J.3
Fodor, S.P.A.4
Gordon, E.M.5
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2
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0029065615
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Combinatorial synthesis: The design of compound libraries and their application to drug discovery
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(b) Terrett, N.K., Gardner, M., Gordon, D.W., Kobylecki, R.J. and Steele, J., Combinatorial synthesis: The design of compound libraries and their application to drug discovery, Tetrahedron, 51 (1995) 8135-8173.
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Terrett, N.K.1
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3
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Synthesis and application of small molecule libraries
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(d) Wessjohann, L.A., Synthesis of natural-product-based compound libraries, Curr. Opin. Chem. Biol., 4 (2000) 303-309.
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0035358567
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Lead compounds discovered from libraries
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(e) Golebiowski, A., Klopfenstein, S.R. and Portlock, D.E., Lead compounds discovered from libraries, Curr. Opin. Chem. Biol., 5 (2001) 273-284.
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Golebiowski, A.1
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6
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0035108339
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Antitumor activity of benzamide ribside and its combination with cisplatin and staurosporine
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For antitumor activity of amides, see: (a) Rauko, P., Novotny, L., Dovinova, I., Hunakova, L., Szekeres, T. and Jayaram, H. N., Antitumor activity of benzamide ribside and its combination with cisplatin and staurosporine, Eur. J. Pharm. Sci., 12 (2001) 387-394.
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Rauko, P.1
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Hunakova, L.4
Szekeres, T.5
Jayaram, H.N.6
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7
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0033490799
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Synthesis, characterization and anticonvulsant activity of enaminones. Part 6: Synthesis of substituted vinylic benzamides as potential anticonvulsants
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(b) Anticonvulsant activity reported as: Foster, J.E., Nicholson, J.M., Butcher, R., Stables, J.P., Edafiogho, I.O., Goodwin, A.M., Henson, M.C. and Smith, C.A., Synthesis, characterization and anticonvulsant activity of enaminones. Part 6: Synthesis of substituted vinylic benzamides as potential anticonvulsants, Bioorganic. Med. Chem., 7 (1999) 2415-2425.
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Foster, J.E.1
Nicholson, J.M.2
Butcher, R.3
Stables, J.P.4
Edafiogho, I.O.5
Goodwin, A.M.6
Henson, M.C.7
Smith, C.A.8
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8
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0033671140
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Synthesis and microbiological activity of some N-(c-hydroxylphenyl)benzamides and phenylacetamides as the possible metabolites of antimicrobial active benzoxazoles: Part II
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(c) For antimicrobile activity of amides, see: Sener, E.A., Bingöl, K.K., Ören, I., Arpaci, Ö. T., Yalçin, Ì. and Altanlar, N., Synthesis and microbiological activity of some N-(c-hydroxylphenyl)benzamides and phenylacetamides as the possible metabolites of antimicrobial active benzoxazoles: Part II, II Farmaco, 55 (2000) 469-476.
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II Farmaco
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Sener, E.A.1
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Arpaci, Ö.T.4
Yalçin, Ì.5
Altanlar, N.6
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9
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0033580080
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A QSAR study of the antiallergic activities of substitute benzamides and their structures
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(d) For antiallergic activity of amides, see: Zhou, Y.X., Xu, L., Wu, Y.P. and Liu, B.L., A QSAR study of the antiallergic activities of substitute benzamides and their structures, Chemom. Intell. Lab. Syst., 45 (1999) 95-100.
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Zhou, Y.X.1
Xu, L.2
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0030680993
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Secondary amide-based linkers for solid phase organic synthesis
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Swayze, E.E., Secondary amide-based linkers for solid phase organic synthesis, Tetrahedron Lett., 38 (1997) 8465-8468.
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Swayze, E.E.1
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0029918554
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Synthesis of an array of amides by aluminium chloride assisted cleavage of resin-bound esters
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Barn, D.R., Morphy, J.R. and Rees, D.C., Synthesis of an array of amides by aluminium chloride assisted cleavage of resin-bound esters, Tetrahedron Lett., 37 (1996) 3213-3216.
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Barn, D.R.1
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0030747024
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Reagents for combinatorial organic synthesis: Preparation and uses of Rink-chloride
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Garigipati, R.S., Reagents for combinatorial organic synthesis: Preparation and uses of Rink-chloride, Tetrahedron Lett., 38 (1997) 6807-6810.
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Garigipati, R.S.1
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0029145404
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Reductive alkylation of 9-amino-xanthen-3-yloxymethylpoly (styrene): A novel procedure for the synthesis of peptidyl N-alkyl amides by Fmoc/But chemistry
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Chan, W.C. and Mellor, S.L., Reductive alkylation of 9-amino-xanthen-3-yloxymethylpoly (styrene): A novel procedure for the synthesis of peptidyl N-alkyl amides by Fmoc/But chemistry, J. Chem. Soc. Chem. Commun., (1995) 1475-1477.
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Chan, W.C.1
Mellor, S.L.2
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0030658101
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An AMEBA acid sensitive aldehyde resin for solid phase synthesis
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Fivush, A.M. and Willson, T.M., AMEBA: An acid sensitive aldehyde resin for solid phase synthesis, Tetrahedron Lett., 38 (1997) 7151-7154.
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Fivush, A.M.1
Willson, T.M.2
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0030817703
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Solid phase synthesis of secamides and removal from the polymeric support under mild conditions
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Sarantakis, D. and Bicksler, J.J., Solid phase synthesis of secamides and removal from the polymeric support under mild conditions, Tetrahedron Lett., 38 (1997) 7325-7328.
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Sarantakis, D.1
Bicksler, J.J.2
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16
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0032499988
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Immobilized aldehydes and olefins in the solid support synthesis of tetrahydroquinolines via a three component condensation
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Kiselyov, A.S., Smith Jr., L., Virgilio, A. and Armstrong, R.W., Immobilized aldehydes and olefins in the solid support synthesis of tetrahydroquinolines via a three component condensation, Tetrahedron, 54 (1998) 7987-7996.
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Tetrahedron
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Kiselyov, A.S.1
Smith L., Jr.2
Virgilio, A.3
Armstrong, R.W.4
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17
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0032503569
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Backbone amide linker (BAL) strategy for solid phase synthesis of C-terminal-modified and cyclic pepetides
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Jensen, K.J., Alsina, J., Songster, M.F., Vagner, J., Albericio, F. and Barany, G., Backbone amide linker (BAL) strategy for solid phase synthesis of C-terminal-modified and cyclic pepetides, J. Am. Chem. Soc., 120 (1998) 5441-5452.
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Barany, G.6
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18
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0030932342
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Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality
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Boojamra, C.G., Burow, K.M., Thompson, L.A. and Ellman, J.A., Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality, J. Org. Chem., 62 (1997) 1240-1256.
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0011667653
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Indole resin: A versatile new support for the solid-phase synthesis of organic molecules
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Estep, K.G., Neipp, C.E., Stramiello, L.M.S., Adam, M.D., Allen, M.P., Robinson, S. and Roskamp, E.J., Indole resin: A versatile new support for the solid-phase synthesis of organic molecules, J. Org. Chem., 63 (1998) 5300-5301.
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Robinson, S.6
Roskamp, E.J.7
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20
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0025783278
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Synthesis of peptide analogs using the multipin peptide synthesis method
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Valerio, R.M., Benstead, M., Bray, A.M., Campbell, R.A. and Maeji, N.J., Synthesis of peptide analogs using the multipin peptide synthesis method, Anal. Biochem. 197 (1991) 168-177.
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21
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0026532674
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Preparation of protected peptide amides using the Fmoc chemical protocol. Comparison of the resins for solid phase synthesis
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Story, S.C. and Aldrich, J.V., Preparation of protected peptide amides using the Fmoc chemical protocol. Comparison of the resins for solid phase synthesis, Int. J. Peptide Protein Res., 39 (1992) 87-92.
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Pictet-spengler reaction on solid support
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Yang, L.1
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0030883636
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Solid-phase synthesis of artificial beta-sheets
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Holmes, D.L., Smith, E.M. and Nowick, J.S., Solid-phase synthesis of artificial beta-sheets, J. Amer. Chem. Soc., 119 (1997) 7665-7669.
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0028153553
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A convenient solid phase preparation of peptides substituted amides
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Voyer, N., Lavoie, A., Pinette, M. and Bernier, J., A convenient solid phase preparation of peptides substituted amides, Tetrahedron Lett., 35 (1994) 355-358.
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Safety catch principle in solid phase peptide synthesis
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Kenner, G.W., Mcdermott, J.R. and Sheppard, R.C., Safety catch principle in solid phase peptide synthesis, J. Chem. Soc. Chem. Commun., 12 (1971), 636-637.
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0000246280
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Carbon-carbon bond-forming methods on solid support. Utilization of Kenner's 'safety-catch' linker
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(a) Backes, B.J. and Ellman, J.A., Carbon-carbon bond-forming methods on solid support. Utilization of Kenner's 'safety-catch' linker, J. Am. Chem. Soc., 116 (1994) 11171-11172.
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Activation method to prepare a highly reactive acylsulfonamide 'safety-catch' linkerfor solid-phase synthesis
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0032537689
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Practical method for the parallel synthesis of 2′-amido-2′-deoxyadenosines
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Link, A., Van Calenbergh, S. and Herdewijin, P., Practical method for the parallel synthesis of 2′-amido-2′-deoxyadenosines, Tetrahedron Lett., 39 (1998) 5175-5176.
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Link, A.1
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An alkanesulfoamide 'safety-catch' Linker for solid-phase synthesis
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Backes, B.J. and Ellman, J.A., An alkanesulfoamide 'safety-catch' Linker for solid-phase synthesis, J. Org. Chem., 64 (1999) 2322-2330.
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Nájera, C. and Yus, M., Desulfonylation reactions: Recent developments, Tetrahedron, 55 (1999) 10547-10658.
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Nájera, C.1
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A radical approach to N-desulfonylation
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(a) Parsons, A.F. and Pettifer, R.M., A radical approach to N-desulfonylation, Tetrahedron Lett., 37 (1996) 1667-1670.
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(b) Knowles, H., Parsons, A.F. and Pettifer, R.M., Desulfonylation of amides using samarium iodide, Synlett., (1997) 271-272.
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Desulfonylation of amides using tributylin hydride, samarium diiodide or zinc/titanium, tetrachloride. A comparison of methods
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(c) Knowles, H.S., Parsons, A.F., Pettifer, R.M. and Rickling, S., Desulfonylation of amides using tributylin hydride, samarium diiodide or zinc/titanium, tetrachloride. A comparison of methods, Tetrahedron, 56 (2000) 979-988.
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0001563784
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An efficient new method for the desulfonylation of β-keto phenylsulfones
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A similar mechanism for desulfonylation of β-keto phenylsulfones were porposed in following papers: (d) Smith, A.B., Hale, K.J. and McCauley, J.P., An efficient new method for the desulfonylation of β-keto phenylsulfones, Tetrahedron Lett., 30 (1989) 5579-5582.
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Smith, A.B.1
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Application of diffuse reflectance IR spectroscopy technique in optimizing synthesis of 2-polystyrylsulfonamidoethanol
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Luo, J.T., Huang, W.Q. and Wu, Q., Application of diffuse reflectance IR spectroscopy technique in optimizing synthesis of 2-polystyrylsulfonamidoethanol, Lizijiaohuan yu Xifu (Ion Exchange and Adsorption), 18 (2002) 85-88.
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