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The Journal of Organic Chemistry|September 12, 2008
Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTfMichio Kurosu, Kai LiMolecules (Basel, Switzerland)|March 26, 2010
Vitamin K2 in electron transport system: are enzymes involved in vitamin K2 biosynthesis promising drug targets?Michio Kurosu, Eeshwaraiah BegariOrganic Letters|January 28, 2009
New chiral derivatizing agents: convenient determination of absolute configurations of free amino acids by 1H NMRMichio Kurosu, Kai LiHeterocycles|December 15, 2012
MILD AND SELECTIVE O-GLYCOSYLATIONS OF PRIMARY ALCOHOLS WITH THE THIOGLUCOSAMINIDE DERIVATIVE PROMOTED BY N-IODOSUCCINIMIDE AND HBF(4)-ADOSROBED ON SILICA GELMichio Kurosu, Kai LiTetrahedron|June 20, 2012
A new protecting group and linker for uridine ureido nitrogenYong Wang, Michio KurosuMolecules (Basel, Switzerland)|October 29, 2025
DPAGT1-Perspective as an Anticancer Drug TargetMichio Kurosu, Katsuhiko MitachiMedicinal Chemistry (Shariqah (United Arab Emirates))|March 12, 2009
MenA is a promising drug target for developing novel lead molecules to combat Mycobacterium tuberculosisMichio Kurosu, Dean C CrickBioorganic & Medicinal Chemistry Letters|May 10, 2006
Small-molecule microarrays: development of novel linkers and an efficient detection method for bound proteinsMichio Kurosu, Williams A MowersTetrahedron Letters|June 20, 2012
A reliable Pd-mediated hydrogenolytic deprotection of BOM group of uridine ureido nitrogenBilal A Aleiwi, Michio KurosuSynthesis|April 18, 2022
A Convenient Protecting Group for Uridine Ureido Nitrogen: (4,4'-Bisfluorophenyl)methoxymethyl groupKatsuhiko Mitachi, David Mingle, Michio KurosuPageof 5