Synthesis and fungicidal activity of N-2-(3-methoxy-4-propargyloxy) phenethyl amides. Part II: anti-oomycetic mandelamides
Lamberth C., Cederbaum F., Jeanguenat A., Kempf H., Zeller M., Zeun R. (2006) Synthesis and fungicidal activity of N-2-(3-methoxy-4-propargyloxy) phenethyl amides. Part II: anti-oomycetic mandelamides. Pest Manag Sci;62:446-451.
A quantitative PCR assay for detection of Xanthomonas fragariae. A quantitative PCR assay for detection of Xanthomonas fragariae.
Hsu C., McCallister J., Hartung J., Turechek W. (2006) A quantitative PCR assay for detection of Xanthomonas fragariae. A quantitative PCR assay for detection of Xanthomonas fragariae. p. S51.
Mandipropamid targets the cellulose synthase-like PiCesA3 to inhibit cell wall biosynthesis in the oomycete plant pathogen, Phytophthora infestans
Blum M., Boehler M., Randall E., Young V., Csukai M., Kraus S., Moulin F., Scalliet G., Avrova A.O., Whisson S.C. (2010) Mandipropamid targets the cellulose synthase-like PiCesA3 to inhibit cell wall biosynthesis in the oomycete plant pathogen, Phytophthora infestans. Mol Plant Pathol;11:227-243.
A stepwise huisgen cycloaddition process: copper (i)-catalyzed regioselective "ligation" of azides and terminal alkynes
Rostovtsev V., Green L., Fokin V., Sharpless K. (2002) A stepwise huisgen cycloaddition process: copper (i)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew Chem Int Ed;41:2596-2599.
Click linker: efficient and high-yielding synthesis of a new family of SPOS resins by 1, 3-dipolar cycloaddition
Lober S., Rodriguez-Loaiza P., Gmeiner P. (2003) Click linker: efficient and high-yielding synthesis of a new family of SPOS resins by 1, 3-dipolar cycloaddition. Org Lett;5:1753-1755.
Highlights in organic chemistry advances in 1, 3-dipolar cycloaddition reaction of azides and alkynes-A prototype of click chemistry
Wang Q., Chittaboina S., Barnhill H. (2005) Highlights in organic chemistry advances in 1, 3-dipolar cycloaddition reaction of azides and alkynes-A prototype of click chemistry. Lett Org Chem;2:293-301.
CuI-catalyzed alkyne-azide "click" cycloadditions from a mechanistic and synthetic perspective
Bock V., Hiemstra H., van Maarseveen J. (2006) CuI-catalyzed alkyne-azide "click" cycloadditions from a mechanistic and synthetic perspective. Eur J Org Chem;2006:51-68.
1, 2, 3-Triazole as a peptide surrogate in the rapid synthesis of HIV-1 protease inhibitors
Brik A., Alexandratos J., Lin Y., Elder J., Olson A., Wlodawer A. et al. (2005) 1, 2, 3-Triazole as a peptide surrogate in the rapid synthesis of HIV-1 protease inhibitors. ChemBioChem;6:1167-1169.
Click chemistry reactions in medicinal chemistry: applications of the 1, 3-dipolar cycloaddition between azides and alkynes
Tron G., Pirali T., Billington R., Canonico P., Sorba G., Genazzani A. (2008) Click chemistry reactions in medicinal chemistry: applications of the 1, 3-dipolar cycloaddition between azides and alkynes. Med Res Rev;28:278-308.
Rapid assembly of matrix metalloprotease inhibitors using click chemistry
Wang J., Uttamchandani M., Li J., Hu M., Yao S. (2006) Rapid assembly of matrix metalloprotease inhibitors using click chemistry. Org Lett;8:3821-3824.
"Click" synthesis of small molecule probes for activity-based fingerprinting of matrix metalloproteases
Wang J., Uttamchandani M., Li J., Hu M., Yao S. (2006) "Click" synthesis of small molecule probes for activity-based fingerprinting of matrix metalloproteases. Chem Commun (Camb);2006:3783-3785.
Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors
Brik A., Muldoon J., Lin Y., Elder J., Goodsell D., Olson A. et al. (2003) Rapid diversity-oriented synthesis in microtiter plates for in situ screening of HIV protease inhibitors. ChemBioChem;4:1246-1248.
Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvage
Galli U., Ercolano E., Carraro L., Roman C., Sorba G., Canonico P. et al. (2008) Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvage. ChemMedChem;3:771-779.
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
Whiting M., Tripp J., Lin Y., Lindstrom W., Olson A., Elder J. et al. (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.
A copper (II)-catalyzed Aza-Friedel̈CCrafts reaction of N-(2-Pyridyl) sulfonyl aldimines: synthesis of unsymmetrical diaryl amines and triaryl methanes
Esquivias J., Gómez Arrayás R., Carretero J. (2006) A copper (II)-catalyzed Aza-Friedel̈CCrafts reaction of N-(2-Pyridyl) sulfonyl aldimines: synthesis of unsymmetrical diaryl amines and triaryl methanes. Angew Chem Int Ed;45:629-633.
Rapid assembly and in situ screening of bidentate inhibitors of protein tyrosine phosphatases
Srinivasan R., Uttamchandani M., Yao S. (2006) Rapid assembly and in situ screening of bidentate inhibitors of protein tyrosine phosphatases. Org Lett;8:713-716.
Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide
Kim S., Cho M., Lee T., Lee S., Min H., Lee S. (2007) Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide. Bioorg Med Chem Lett;17:4584-4587.
New recurrent synthetic method for the synthesis of functionalized oligomeric [beta]-O-4 lignin model compounds
Roblin J., Duran H., Duran E., Banuls V., Gorrichon L. (1996) New recurrent synthetic method for the synthesis of functionalized oligomeric [beta]-O-4 lignin model compounds. Bioorg Med Chem Lett;6:2355-2358.
Total synthesis and biological evaluation of viscolin, a 1, 3-diphenylpropane as a novel potent anti-inflammatory agent
Su C., Shen Y., Kuo P., Leu Y., Damu A., Wang Y. et al. (2006) Total synthesis and biological evaluation of viscolin, a 1, 3-diphenylpropane as a novel potent anti-inflammatory agent. Bioorg Med Chem Lett;16:6155-6160.
Design, synthesis and antiproliferative activity of tripentones: a new series of antitubulin agents
Lisowski V., Enguehard C., Lancelot J., Caignard D., Lambel S., Leonce S. et al. (2001) Design, synthesis and antiproliferative activity of tripentones: a new series of antitubulin agents. Bioorg Med Chem Lett;11:2205-2208.
Synthesis and biological activities of 3-substituent-5-aryl-4-oxazolidinones
Yao H.-W., Li H.-H., Su N.-N., Wang H.-X., Liu X.-H., Wang L.-Z. et al. (2009) Synthesis and biological activities of 3-substituent-5-aryl-4-oxazolidinones. Chem J Chin Univ;30:908-912.