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The Journal of Organic Chemistry|November 2, 2010
A diastereoselective three-component coupling approach to highly substituted pyrrolidinesMani Raj Chaulagain, Zachary D AronOrganic Letters|September 13, 2011
Efficient, single-step access to imidazo[1,5-a]pyridine n-heterocyclic carbene precursorsJohnathon T Hutt, Zachary D AronChemical Communications (Cambridge, England)|January 24, 2004
The tethered Biginelli condensation in natural product synthesisZachary D Aron, Larry E OvermanOrganic Letters|February 25, 2005
Stereocontrolled synthesis of angularly substituted 1-azabicyclic rings by cationic 2-aza-cope rearrangementsZachary D Aron, Larry E OvermanJournal of the American Chemical Society|March 10, 2005
Total synthesis and properties of the crambescidin core zwitterionic acid and crambescidin 359Zachary D Aron, Larry E OvermanOrganic Letters|April 7, 2010
Simplifying pyridoxal: practical methods for amino acid dynamic kinetic resolutionAlbert E Felten, Gangguo Zhu, Zachary D AronOrganic Letters|April 11, 2012
Catalytic α-allylation of unprotected amino acid estersPing Fang, Mani Raj Chaulagain, Zachary D AronJournal of the American Chemical Society|February 10, 2009
Cascade reactions during coronafacic acid biosynthesis: elongation, cyclization, and functionalization during Cfa7-catalyzed condensationEric R Strieter, Alexander Koglin, Zachary D Aron, et al.The Journal of Organic Chemistry|August 20, 2013
Diastereo- and enantioselective three-component coupling approach to highly substituted pyrrolidinesMani Raj Chaulagain, Albert E Felten, Kevin Gilbert, et al.Bioorganic & Medicinal Chemistry Letters|June 5, 2004
Synthesis and anticancer activity of side chain analogs of the crambescidin alkaloidsZachary D Aron, Halina Pietraszkiewicz, Larry E Overman, et al.Pageof 2