Chemoselective Arylamidine Cyclizations:  Mild Formation of 2-Arylimidazole-4-carboxylic Acids von Yoburn, Joshua C, Baskaran, Subramanian

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Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitors von Fucini, Raymond V., Hanan, Emily J., Romanowski, Michael J., Elling, Robert A., Lew, Willard, Barr, Kenneth J., Zhu, Jiang, Yoburn, Joshua C., Liu, Yang, Fahr, Bruce T., Fan, Junfa, Lu, Yafan, Pham, Phuongly, Choong, Ingrid C., VanderPorten, Erica C., Bui, Minna, Purkey, Hans E., Evanchik, Marc J., Yang, Wenjin

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Synthesis of Dityrosine Cross-Linked Peptide Dimers Using the Miyaura−Suzuki Reaction von Yoburn, Joshua C, Van Vranken, David L

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Dityrosine Cross-Linked Aβ Peptides:  Fibrillar β-Structure in Aβ(1-40) Is Conducive to Formation of Dityrosine Cross-Links but a Dityrosine Cross-Link in Aβ(8-14) Does Not Induce... von Yoburn, Joshua C, Tian, Wenqiang, Brower, Justin O, Nowick, James S, Glabe, Charles G, Van Vranken, David L

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Synthesis and study of a gramicidin B mutant possessing a ditryptophan crosslink von Presley Bodnar, Alice L., Gilbert, Eric J., Yoburn, Joshua C., Van Vranken, David L.

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Indolocarbazole Glycosides in Inactive Conformations von Facompré, Michaël, Carrasco, Carolina, Vezin, Hervé, Chisholm, John D, Yoburn, Joshua C, Van Vranken, David L, Bailly, Christian

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A biaryl peptide crosslink in a MetJ peptide model confers cooperative, nonspecific binding to DNA that ablates both repressor binding and In vitro transcription von Yoburn, Joshua C, Deb, Sipra, Manfield, Iain W, Stockley, Peter G, Vranken, David L.Van

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Dityrosine cross-linked Abeta peptides: fibrillar beta-structure in Abeta(1-40) is conducive to formation of dityrosine cross-links but a dityrosine cross-link in Abeta(8-14) does... von Yoburn, Joshua C, Tian, Wenqiang, Brower, Justin O, Nowick, James S, Glabe, Charles G, Van Vranken, David L

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Chemoselective Arylamidine Cyclizations: Mild Formation of 2-Arylimidazole-4-carboxylic Acids von Yoburn, Joshua C., Baskaran, Subramanian

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THIENOPYRIMIDINES USEFUL AS AURORA KINASE INHIBITORS von LEW WILLARD, ZHONG MIN, BASKARAN SUBRAMANIAN, OSLOB JOHAN D, YOBURN JOSHUA C

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Thienopyrimidines useful as Aurora kinase inhibitors von Lew, Willard, Baskaran, Subramanian, Oslob, Johan D, Yoburn, Joshua C, Zhong, Min

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Thienopyrimidines useful as Aurora kinase inhibitors von LEW WILLARD, ZHONG MIN, BASKARAN SUBRAMANIAN, OSLOB JOHAN D, YOBURN JOSHUA C

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Thienopyrimidines useful as Aurora kinase inhibitors von LEW WILLARD, ZHONG MIN, BASKARAN SUBRAMANIAN, OSLOB JOHAN D, YOBURN JOSHUA C

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Synthesis and structure-activity relationships of pyridoxal-6-arylazo-5′-phosphate and phosphonate derivatives as P2 receptor antagonists von Kim, Yong-Chul, Camaioni, Emidio, Ziganshin, Airat U., Ji, Xiao-duo, King, Brian F., Wildman, Scott S., Rychkov, Alexei, Yoburn, Joshua, Kim, Heaok, Mohanram, Arvind, Harden, T. Kendall, Boyer, José L., Burnstock, Geoffrey, Jacobson, Kenneth A.

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