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Journal of the American Chemical Society|October 23, 2003
Total syntheses of furaquinocin A, B, and EBarry M Trost, Oliver R Thiel, Hon-Chung TsuiJournal of the American Chemical Society|September 26, 2002
DYKAT of Baylis-Hillman adducts: concise total synthesis of furaquinocin EBarry M Trost, Oliver R Thiel, Hon-Chung TsuiChemical Science|April 29, 2017
Co/NHPI-mediated aerobic oxygenation of benzylic C-H bonds in pharmaceutically relevant moleculesDamian P Hruszkewycz, Kelsey C Miles, Oliver R Thiel, et al.The Journal of Organic Chemistry|February 28, 2009
An efficient and scalable Ritter reaction for the synthesis of tert-butyl amidesJean C Baum, Jacqueline E Milne, Jerry A Murry, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|July 28, 2011
Total synthesis of bryostatins: the development of methodology for the atom-economic and stereoselective synthesis of the ring C subunitBarry M Trost, Alison J Frontier, Oliver R Thiel, et al.Journal of the American Chemical Society|July 22, 2015
Pyridine N-Oxide vs Pyridine Substrates for Rh(III)-Catalyzed Oxidative C-H Bond FunctionalizationSharon R Neufeldt, Gonzalo Jiménez-Osés, John R Huckins, et al.Journal of the American Chemical Society|September 12, 2013
Rh(III)-catalyzed C-H activation and double directing group strategy for the regioselective synthesis of naphthyridinonesJohn R Huckins, Eric A Bercot, Oliver R Thiel, et al.The Journal of Organic Chemistry|July 30, 2008
Selective ortho methylation of nitroheteroaryls by vicarious nucleophilic substitutionMichał Achmatowicz, Oliver R Thiel, Gilles Gorins, et al.The Journal of Organic Chemistry|December 18, 2008
Practical synthesis of a p38 MAP kinase inhibitorMichał Achmatowicz, Oliver R Thiel, Philip Wheeler, et al.The Journal of Organic Chemistry|March 21, 2008
Practical synthesis of a vanilloid receptor-1 antagonistOliver R Thiel, Charles Bernard, Tony King, et al.Pageof 2