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Yang, K.1
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2
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0037156678
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Solid-phase parallel synthesis of 2-aminoimidazolidin-4-ones
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Yu, Y.1
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3
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0037012923
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A solid-phase synthesis of 1,5-disubstituted 2-aryliminolmidazolidines
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Yu, Y.1
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5
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0037060064
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Solid-phase parallel synthesis of substituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts
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Acharya AN, Ostresh JM, Houghten RA: Solid-phase parallel synthesis of substituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts. Tetrahedron Lett (2002) 43(7):1157-1160. This paper features a solid-phase synthesis involving 11 steps.
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Acharya, A.N.1
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0037189093
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A traceless solid-phase synthesis of 2-imidazolones
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Cheng, J.-F.1
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7
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0037182278
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Solid-phase synthesis of functionalized 1,2,3-triazoles
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Blass, B.E.1
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8
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0037012920
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Peptidotriazoles on solid-phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
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Tornoe CW, Christensen C, Meldal M: Peptidotriazoles on solid-phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J Org Chem (2002) 67(9):3057-3064.
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J Org Chem
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Tornoe, C.W.1
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0037140842
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Solid-phase synthesis of 1,2,4-triazolidine-3,5-diones
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Park KH, Cox LJ: Solid-phase synthesis of 1,2,4-triazolidine-3,5-diones. Tetrahedron Lett (2002) 43(21):3899-3901.
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Park, K.H.1
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Solid support synthesis of 2,4-disubstituted thiazoles and aminothiazoles
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Kazzouli, S.E.1
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11
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0038480375
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Stieber F, Mazitschek R, Soric N, Giannis A, Waldmann H: Traceless solid-phase synthesis of 2-aminothiazoles: Receptor tyrosine kinase inhibitors with dual selectivity for Tie-2 and VEGFR-2. Angew Chem Chem Int Ed (2002) 41(24):4757-4761. Use of Hantzsch synthesis in solid-phase synthesis.
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Angew Chem Chem Int Ed
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Stieber, F.1
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Waldmann, H.5
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12
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0037057584
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Parallel synthesis of potent, pyrazole-based inhibitors of Helicobacter pylori dihydroorotate dehydrogenase
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1 < 10 nM against H pylori DHODase and > 10,000-fold selectivity over human DHODase were obtained.
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J Med Chem
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Haque, T.S.1
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13
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Synthetic applications of azolium ylides to a traceless solid-phase synthesis of 2-substituted azoles
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Org Lett
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Deng, Y.1
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0037047538
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A traceless approach for the parallel solid-phase synthesis of 2-(arylamino) quinazolinones
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Yu Y, Ostresh JM, Houghten RA: A traceless approach for the parallel solid-phase synthesis of 2-(arylamino) quinazolinones. J Org Chem (2002) 67(16):5831-5834.
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J Org Chem
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Yu, Y.1
Ostresh, J.M.2
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15
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0037025731
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Solid-phase synthesis of quinazolin-4(3H)-ones with three-point diversity
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Kesarwani AP, Srivastava GK, Rastogi S, Kundu B: Solid-phase synthesis of quinazolin-4(3H)-ones with three-point diversity. Tetrahedron Lett (2002) 43(32):5579-5581.
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Kesarwani, A.P.1
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16
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0037100096
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Efficient solid-phase synthesis of 2,3-substituted indoles
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Wacker, D.A.1
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Combinatorial synthesis of 3-(amidoalkyl) and (aminoalkyl)-2-arylindole derivatives: Discovery of potent ligands for a variety of G-protein coupled receptors
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Willoughby CA, Hutchins SM, Rosauer KG, Dhar MJ, Chapman KT, Chicchi GG, Sadowski S, Weinberg DH, Patel S, Malkowitz L, Salvo JD et al: Combinatorial synthesis of 3-(amidoalkyl) and (aminoalkyl)-2-arylindole derivatives: Discovery of potent ligands for a variety of G-protein coupled receptors. Bioorg Med Chem Lett (2002) 12(1):93-96. A library of 12,800 compounds as 320 pools of 400 compounds was synthesized.
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Bioorg Med Chem Lett
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Willoughby, C.A.1
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18
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0037048495
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Pictet-Spengler synthesis of tetrahydro-β-carbolines using vinylsulfonylmethyl resin
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Connors RV, Zhang AJ, Shuttleworth SJ: Pictet-Spengler synthesis of tetrahydro-β-carbolines using vinylsulfonylmethyl resin. Tetrahedron Lett (2002) 43(37):6661-6663. The use of vinylsulfonylmethyl resin for Pictet-Spengler synthesis is described.
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Connors, R.V.1
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19
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0040077869
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Solid-phase synthesis of 4,6-disubstituted and 3,4,6-trisubstituted pyrid-2-ones
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J Combinatorial Chem
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Katritzky, A.R.1
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20
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0040671363
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Solid-phase synthesis of imidazo[4,5-b]pyridin-2-ones and related urea derivatives by cyclative cleavage of a carbamate linkage
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Ermann M, Simkovsky NM, Roberts SM, Parry DM, Baxter AD: Solid-phase synthesis of imidazo[4,5-b]pyridin-2-ones and related urea derivatives by cyclative cleavage of a carbamate linkage. J Combinatorial Chem (2002) 4(2):352-358.
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J Combinatorial Chem
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0036831916
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Solid-phase synthesis of isoxazolines
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Chandrasekar S, Raza A, Reddy MV, Yadav JS: Solid-phase synthesis of isoxazolines. J Combinatorial Chem (2002) 4(6):652-655.
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J Combinatorial Chem
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Chandrasekar, S.1
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0037031635
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Versatile 'traceless' sulfone linker for SPOS: Preparation of isoxazolinopyrrole-2-carboxylates
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Hwang SH, Kurth MJ: Versatile 'traceless' sulfone linker for SPOS: Preparation of isoxazolinopyrrole-2-carboxylates. J Org Chem (2002) 67(18):6564-6567.
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J Org Chem
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Hwang, S.H.1
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Solid-phase synthesis of unsaturated 3-substituted piperazine-2,5-diones
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Li WR, Yang JH: Solid-phase synthesis of unsaturated 3-substituted piperazine-2,5-diones. J Combinatorial Chem (2002) 4:106-108.
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J Combinatorial Chem
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Li, W.R.1
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0036832823
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Parallel solid-phase synthesis of disubstituted 1,6-piperazine-2-ones
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J Combinatorial Chem
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Nefzi, A.1
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25
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0036066524
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A cyclative cleavage approach to the solid-phase synthesis of 2-oxo-1,4-piperazines
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0037042770
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A library construction of 2,5-disubstituted pyrrole compounds by using solid/solution-phase syntheses
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Kobayashi N, Kaku Y, Higurashi K, Yamauchi T, Ishibashi A, Okamoto Y: A library construction of 2,5-disubstituted pyrrole compounds by using solid/solution-phase syntheses. Bioorg Med Chem Lett (2002) 12(13):1747-1750.
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27
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0037020713
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Parallel solution-and solid-phase synthesis of spiropyrrolo-pyrroles as novel neurokinin receptor ligands
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Bleicher KH, Wuthrich Y, Adam G, Hoffmann T, Sleight AJ: Parallel solution-and solid-phase synthesis of spiropyrrolo-pyrroles as novel neurokinin receptor ligands. Bioorg Med Chem Lett (2002) 12(21):3073-3076.
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Bioorg Med Chem Lett
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Bleicher, K.H.1
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0037181078
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A combinatorial scaffold approach toward kinase-directed heterocycle libraries
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Ding S, Gray NS, Wu X, Ding Q, Schultz PG: A combinatorial scaffold approach toward kinase-directed heterocycle libraries. J Am Chem Soc (2002) 124(8):1594-1596. The preparation of diverse heterocyclic libraries by using seven dichloroheterocyclic scaffolds is presented.
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J Am Chem Soc
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Ding, S.1
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0037144639
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Solid-phase synthesis of 4(1H)-quinolone and pyrimidine derivatives based on a new scaffold-polymer-bound cyclic malonic acid ester
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Huang X, Liu Z: Solid-phase synthesis of 4(1H)-quinolone and pyrimidine derivatives based on a new scaffold-polymer-bound cyclic malonic acid ester. J Org Chem (2002) 67(19):6731-6737. This paper deals with a selection of common combinatorial scaffold for the synthesis of a variety of heterocyclic compounds.
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J Org Chem
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Huang, X.1
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Solid-phase synthesis of 'diverse' heterocycles
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Purandare AV, Gao A, Poss MA: Solid-phase synthesis of 'diverse' heterocycles. Tetrahedron Lett (2002) 43(21):3903-3906. A selection of a common combinatorial intermediate for the synthesis of a variety of heterocyclic compounds is presented.
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Tetrahedron Lett
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Purandare, A.V.1
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