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Journal of the American Chemical Society|May 17, 2017
Scalable, Electrochemical Oxidation of Unactivated C-H BondsYu Kawamata, Ming Yan, Zhiqing Liu, et al.Journal of the American Chemical Society|June 17, 2004
Direct coupling of indoles with carbonyl compounds: short, enantioselective, gram-scale synthetic entry into the hapalindole and fischerindole alkaloid familiesPhil S Baran, Jeremy M RichterJournal of the American Chemical Society|July 4, 2002
A short synthetic route to (+)-austamide, (+)-deoxyisoaustamide, and (+)-hydratoaustamide from a common precursor by a novel palladium-mediated indole --> dihydroindoloazocine cyclizationPhil S Baran, E J CoreyIsrael Journal of Chemistry|July 25, 2015
Terpenoid-Alkaloids: Their Biosynthetic Twist of Fate and Total SynthesisEmily C Cherney, Phil S BaranChemical Society Reviews|February 8, 2011
C-H functionalization logic in total synthesisWill R Gutekunst, Phil S BaranJournal of the American Chemical Society|March 23, 2006
Total synthesis of (+/-)-haouamine APhil S Baran, Noah Z BurnsAngewandte Chemie (International Ed. in English)|August 31, 2002
The CP molecule labyrinth: a paradigm of how endeavors in total synthesis lead to discoveries and inventions in organic synthesisK C Nicolaou, Phil S BaranThe Journal of Organic Chemistry|February 20, 2014
Applications of C-H functionalization logic to cyclobutane synthesisWill R Gutekunst, Phil S BaranNature Chemistry|March 8, 2011
Protecting-group-free synthesis as an opportunity for inventionIan S Young, Phil S BaranJournal of the American Chemical Society|November 10, 2011
Total synthesis and structural revision of the piperarborenines via sequential cyclobutane C-H arylationWill R Gutekunst, Phil S BaranPageof 259