Diversity-oriented synthesis: Exploring the intersections between chemistry and biology
doi:10.1038/nchembio0705-74
Tan DS (2005) Diversity-oriented synthesis: exploring the intersections between chemistry and biology. Nat Chem Biol 1:74-84. doi:10.1038/nchembio0705- 74
Can we learn to distinguish between 'drug-like' and 'nondrug-like' molecules?
DOI 10.1021/jm970666c
Ajay, Walters WP, Murcko MA (1998) Can we learn to distinguish between "drug-like" and "nondrug-like" molecules. J Med Chem 41:3314-3324. doi:10.1021/jm970666c (Pubitemid 28406538)
From knowing to controlling: A path from genomics to drugs using small molecule probes
DOI 10.1126/science.1083395
Strausberg RL, Schreiber SL (2003) From knowing to controlling: a pathfrom genomics to drugs using small molecule probes. Science 300:294-295. doi:10.1126/science.1083395 (Pubitemid 36433713)
Diversity-oriented synthesis; A spectrum of approaches and results
DOI 10.1039/b719372f
Spandl RJ, Bender A, Spring DR (2008) Diversity-oriented synthesis; a spectrum of approaches and results. Org Biomol Chem 6:1149-1158. doi:10.1039/B719372F (Pubitemid 351432832)
Diversityoriented synthesis as a tool for the discovery of novel biologically active small molecules
doi:10.1038/ncomms1081
Galloway WRJD, Isidro-Llobet A, Spring DR (2010) Diversityoriented synthesis as a tool for the discovery of novel biologically active small molecules. Nat Commun 1:80-92. doi:10.1038/ncomms1081
Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library
doi:10.1073/pnas.1015268108
Lettsa GM, Diblasia CM, Bauerb RA, Tan DS (2011) Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library. Proc Natl Acad Sci USA 17:6745-6750. doi:10.1073/pnas.1015268108
1, 2, 3-Triazole and its derivatives. Development of methods for the formation of the triazole ring
doi:10.1070/RC2005v074n04ABEH000893
Krivopalov VP, Shkurko OP (2005) 1, 2, 3-Triazole and its derivatives. Development of methods for the formation of the triazole ring. Russ Chem Rev 74:339-379. doi:10.1070/RC2005v074n04ABEH000893
Posaconazole: A potent, extended-spectrum triazole anti-fungal for the treatment of serious fungal infections
DOI 10.1111/j.1368-5031.2004.00167.x
Herbrecht R (2004) Posaconazole: a potent, extended-spectrum triazole anti-fungal for the treatment of serious fungal infections. Int J Clin Pract 58:612. doi:10.1111/j.1368-5031.2004.00167.x (Pubitemid 38996992)
Rapid discovery and structure-activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper(I)-catalyzed synthesis of 1,2,3-triazoles and their further functionalization
DOI 10.1021/jm060754+
Whiting M, Tripp JC, Lin YC, Lindstrom W, Olson AJ, Elder JH, Sharpless KB, Fokin VV (2006) Rapid discovery and structure-activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper (I)-catalyzed synthesis of 1, 2, 3-triazoles and their further functionalization. J Med Chem 49:7697-7710. doi:10.1021/jm060754+ (Pubitemid 46033661)
1, 2, 3-Triazole derivatives as new cannabinoid CB1 receptor antagonists
doi:10.1016/j.bmcl.2008.11.029
Hou DR, Alam S, Kuan TC, Ramanathan M, Lin TP, Hung MS (2009) 1, 2, 3-Triazole derivatives as new cannabinoid CB1 receptor antagonists. Bioorg Med Chem Lett 19:1022-1025. doi:10.1016/j.bmcl.2008.11.029
Synthesis and antiprotozoal activity of cationic 1, 4-diphenyl-1H-1, 2, 3-triazoles
doi:10.1021/jm901178d
Bakunov SA, Bakunova SM, Wenzler T, Ghebru M, Werbovetz KA, Brun R, Tidwell RR (2010) Synthesis and antiprotozoal activity of cationic 1, 4-diphenyl-1H-1, 2, 3-triazoles. J Med Chem 53:254-272. doi:10.1021/jm901178d
Efficient synthesis of 5-fluoroalkylated 1H-1,2,3-triazoles and application of the bromodifluoromethylated triazole to prepare new gem-difluorinated triazole compounds
Peng W, Zhu S (2003) Efficient synthesis of 5-fluoroalkylated 1H-1, 2, 3-triazoles and application of the bromodifluoromethylated triazole to prepare new gem-difluorinated triazole compounds. Synlett 2:187-190. doi:10.1002/chin. 200319131 (Pubitemid 36249933)
Bioconjugation by copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition
DOI 10.1021/ja021381e
Wang Q, Chan TR, Fokin VV, Sharpless KB, Finn M (2003) Bioconjugation by copper (I)-catalyzed azide-alkyne [3+2] cycloaddition. J Am Chem Soc 125:3192-3193. doi:10.1021/ja021381e (Pubitemid 36512443)
A potent and highly selective inhibitor of human α-1,3- fucosyltransferase via click chemistry
DOI 10.1021/ja0302836
Lee LV, Mitchell ML, Huang SJ, Fokin VV, Sharpless KB, Wong CH (2003) A potent and highly selective inhibitor of human á-1, 3-fucosyltransferase via click chemistry. J Am Chem Soc 125:9588-9589. doi:10.1021/ja0302836 (Pubitemid 36975912)
Activity-based protein profiling in vivo using a copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition
DOI 10.1021/ja034490h
Speers AE, Adam GC, Cravatt BF (2003) Activity-based protein profiling in vivo using a copper (I)-catalyzed azide-alkyne [3+2] cycloaddition. J Am Chem Soc 125:4686-4687. doi:10.1021/ja034490h (Pubitemid 36505343)
Synthesis of triazoles from nonactivated terminal alkynes via the three-component coupling reaction using a Pd(0)-Cu(I) bimetallic catalyst
DOI 10.1021/ja034191s
Kamijo S, Jin T, Huo Z, Yamamoto Y (2003) Synthesis of triazoles from nonactivated terminal alkynes via the three-component coupling reaction using a Pd (0)-Cu (I) bimetallic catalyst. J Am Chem Soc 125:7786-7787. doi:10.1021/ja034191s (Pubitemid 36782140)
Regioselective [3+2] cycloaddition of chalcones with a sugar azide: Easy access to 1-(5-deoxy-D-xylofuranos-5-yl)-4, 5-disubstituted-1H-1, 2, 3-triazoles
doi:10.1016/j.carres.2010.04.019
Singh N, Pandey S, Tripathi RP (2011) Regioselective [3+2] cycloaddition of chalcones with a sugar azide: easy access to 1-(5-deoxy-D-xylofuranos-5-yl)- 4, 5-disubstituted-1H-1, 2, 3-triazoles. Carbohydr Res 345:1641-1648. doi:10.1016/j.carres.2010.04.019
Aldol condensations in the absence of solvent: Acceleration of the reaction and enhancement of the stereoselectivity
doi:10.1039/P19900003207
Fumio T, Koichi T, Koki H (1990) Aldol condensations in the absence of solvent: acceleration of the reaction and enhancement of the stereoselectivity. J Chem Soc Perkin Trans 1 1:3207-3209. doi:10.1039/P19900003207
Efficient synthesis of chalcones at room temperature in the presence of potassium phosphate
doi:10. 1134/S107042800707024X
Pore DM, Desai Uday V, Thopate TS, Wadgaonkar PP (2007) Efficient synthesis of chalcones at room temperature in the presence of potassium phosphate. Russ J Org Chem 43:1088-1089. doi:10. 1134/S107042800707024X
Synthetic chalcones as efficient inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase PtpA
doi:10.1016/j.bmcl.2008.09.105
Domeneghini CL, Alessandra M, Sechini CMN, Jose NR, Augusto YR, Marcela P, Javier V, Emilia ZM, Andrea V, Hernan T (2008) Synthetic chalcones as efficient inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase PtpA. Bioorg Med Chem Lett 18:6227-6230. doi:10.1016/j.bmcl.2008.09.105
Synthesis and in vitro microbiological evaluation of an array of biolabile 2-morpholino-N-(4, 6-diarylpyrimidin-2-yl) acetamides
doi:10.1016/j.ejmech.2009.12.068
Kanagarajan V, Thanusu J, Gopalakrishnan M (2010) Synthesis and in vitro microbiological evaluation of an array of biolabile 2-morpholino-N-(4, 6-diarylpyrimidin-2-yl) acetamides. Eur JMed Chem 45:1583-1589. doi:10.1016/j.ejmech.2009.12.068