These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
101 related articles for article (PubMed ID: 12739948)
1. Solution- and solid-phase parallel synthesis of 4-alkoxy-substituted pyrimidines with high molecular diversity. Font D; Heras M; Villalgordo JM J Comb Chem; 2003; 5(3):311-21. PubMed ID: 12739948 [TBL] [Abstract][Full Text] [Related]
2. Parallel solution-phase synthesis of 4-dialkylamino-2-methylsulfonyl-6-vinylpyrimidines. Radi M; Petricci E; Maga G; Corelli F; Botta M J Comb Chem; 2005; 7(1):117-22. PubMed ID: 15638490 [TBL] [Abstract][Full Text] [Related]
3. Solid-phase synthesis of the 2-aminobenzoxazole library using thioether linkage as the safety-catch linker. Hwang JY; Gong YD J Comb Chem; 2006; 8(3):297-303. PubMed ID: 16676998 [TBL] [Abstract][Full Text] [Related]
5. An oxidatively-activated safety catch linker for solid phase synthesis. Davies SG; Mortimer DA; Mulvaney AW; Russell AJ; Skarphedinsson H; Smith AD; Vickers RJ Org Biomol Chem; 2008 May; 6(9):1625-34. PubMed ID: 18421396 [TBL] [Abstract][Full Text] [Related]
6. A three-component reaction for diversity-oriented synthesis of polysubstituted piperidines: solution and solid-phase optimization of the first tandem aza[4+2]/allylboration. Touré BB; Hoveyda HR; Tailor J; Ulaczyk-Lesanko A; Hall DG Chemistry; 2003 Jan; 9(2):466-74. PubMed ID: 12532296 [TBL] [Abstract][Full Text] [Related]
7. Microwave-assisted solution- and solid-phase synthesis of 2-amino-4-arylpyrimidine derivatives. Matloobi M; Kappe CO J Comb Chem; 2007; 9(2):275-84. PubMed ID: 17348733 [TBL] [Abstract][Full Text] [Related]
8. Parallel solution-phase synthesis of a 2,6,8,9-tetrasubstituted purine library via a sulfur intermediate. Liu J; Dang Q; Wei Z; Zhang H; Bai X J Comb Chem; 2005; 7(4):627-36. PubMed ID: 16004508 [TBL] [Abstract][Full Text] [Related]
9. O-N intramolecular acyl migration reaction in the development of prodrugs and the synthesis of difficult sequence-containing bioactive peptides. Sohma Y; Hayashi Y; Skwarczynski M; Hamada Y; Sasaki M; Kimura T; Kiso Y Biopolymers; 2004; 76(4):344-56. PubMed ID: 15386265 [TBL] [Abstract][Full Text] [Related]
10. Studies of chemical selectivity of hapten, reactivity, and skin sensitization potency. 3. Synthesis and studies on the reactivity toward model nucleophiles of the 13C-labeled skin sensitizers, 5-chloro-2-methylisothiazol-3-one (MCI) and 2-methylisothiazol-3-one (MI). Alvarez-Sánchez R; Basketter D; Pease C; Lepoittevin JP Chem Res Toxicol; 2003 May; 16(5):627-36. PubMed ID: 12755592 [TBL] [Abstract][Full Text] [Related]
11. Development of the traceless phenylhydrazide linker for solid-phase synthesis. Stieber F; Grether U; Waldmann H Chemistry; 2003 Jul; 9(14):3270-81. PubMed ID: 12866071 [TBL] [Abstract][Full Text] [Related]
12. Parallel synthesis of potent dopaminergic N-phenyltriazole carboxamides applying a novel click chemistry based phenol linker. Loaiza PR; Löber S; Hübner H; Gmeiner P Bioorg Med Chem; 2009 Aug; 17(15):5482-7. PubMed ID: 19592258 [TBL] [Abstract][Full Text] [Related]
13. Polysubstituted pyridazinones from sequential nucleophilic substitution reactions of tetrafluoropyridazine. Pattison G; Sandford G; Yufit DS; Howard JA; Christopher JA; Miller DD J Org Chem; 2009 Aug; 74(15):5533-40. PubMed ID: 19518071 [TBL] [Abstract][Full Text] [Related]
14. Solid-phase synthesis of a 6-phenylquinolin-2(1H)-one library directed toward nuclear hormone receptors. Ruda M; Kann N; Gordon S; Bergman J; Nelson W; Agback P; Hagberg L; Koehler KF J Comb Chem; 2005; 7(4):567-73. PubMed ID: 16004500 [TBL] [Abstract][Full Text] [Related]
15. Thiophene backbone amide linkers, a new class of easily prepared and highly acid-labile linkers for solid-phase synthesis. Jessing M; Brandt M; Jensen KJ; Christensen JB; Boas U J Org Chem; 2006 Sep; 71(18):6734-41. PubMed ID: 16930022 [TBL] [Abstract][Full Text] [Related]
16. Liquid-phase synthesis of combinatorial libraries based on 7-trifluoromethyl-substituted pyrazolo[1,5-a]pyrimidine scaffold. Dalinger IL; Vatsadse IA; Shevelev SA; Ivachtchenko AV J Comb Chem; 2005; 7(2):236-45. PubMed ID: 15762751 [TBL] [Abstract][Full Text] [Related]
17. New synthetic approach to cyclopenta-fused heterocycles based upon a mild Nazarov reaction. Occhiato EG; Prandi C; Ferrali A; Guarna A; Venturello P J Org Chem; 2003 Dec; 68(25):9728-41. PubMed ID: 14656100 [TBL] [Abstract][Full Text] [Related]
18. Divergent and regioselective synthesis of 1,2,4- and 1,2,5-trisubstituted imidazoles. Delest B; Nshimyumukiza P; Fasbender O; Tinant B; Marchand-Brynaert J; Darro F; Robiette R J Org Chem; 2008 Sep; 73(17):6816-23. PubMed ID: 18681408 [TBL] [Abstract][Full Text] [Related]
19. Synthesis of thieno[2,3-d]pyrimidin-2-ylmethanamine combinatorial library with four diversity points. Bogolubsky AV; Ryabukhin SV; Stetsenko SV; Chupryna AA; Volochnyuk DM; Tolmachev AA J Comb Chem; 2007; 9(4):661-7. PubMed ID: 17530808 [TBL] [Abstract][Full Text] [Related]
20. Nucleophilic substitution at the anomeric position of 1,2-O-isopropylidenefuranose derivatives. A novel stereoselective synthesis of cyclic phosphates analogous to cAMP. Romero M; Hernández L; Quintero L; Sartillo-Piscil F Carbohydr Res; 2006 Dec; 341(18):2883-90. PubMed ID: 17087924 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]