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Journal of the American Chemical Society|March 23, 2006
A synthesis of (+)-saxitoxinJames J Fleming, J Du BoisJournal of the American Chemical Society|July 31, 2007
(+)-saxitoxin: a first and second generation stereoselective synthesisJames J Fleming, Matthew D McReynolds, J Du BoisJournal of the American Chemical Society|February 20, 2003
Novel iminium ion equivalents prepared through C-H oxidation for the stereocontrolled synthesis of functionalized propargylic amine derivativesJames J Fleming, Kristin Williams Fiori, J Du BoisOrganic Letters|February 14, 2002
Stereoselective organozinc addition reactions to 1,2-dihydropyrans for the assembly of complex pyran structuresDietrich P Steinhuebel, James J Fleming, J Du BoisOrganic Process Research & Development|August 2, 2011
Rhodium-Catalyzed C-H Amination - An Enabling Method for Chemical SynthesisJ Du BoisMilitary Medicine|May 1, 1992
A technique for subcutaneous knot inversion following running subcuticular closuresJ J Du BoisJournal of the American Chemical Society|November 15, 2002
A unique and highly efficient method for catalytic olefin aziridinationKiran Guthikonda, J Du BoisJournal of the American Chemical Society|July 3, 2010
Ruthenium-catalyzed hydroxylation of unactivated tertiary C-H bondsEric McNeill, J Du BoisOrganic Letters|December 17, 2016
Copper-Catalyzed Oxidative Cyclization of Carboxylic AcidsShyam Sathyamoorthi, J Du BoisJournal of the American Chemical Society|September 18, 2003
A stereoselective synthesis of (-)-tetrodotoxinAndrew Hinman, J Du BoisPageof 10