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Organometallics|April 7, 2021
Preparation of Enantioenriched Alkylcarbastannatranes via Nucleophilic Inversion of Alkyl Mesylates for Use in Stereospecific Cross-Coupling ReactionsGlenn Ralph, Mark R BiscoeJournal of the American Chemical Society|October 16, 2003
Hydrophobically directed selective reduction of ketonesMark R Biscoe, Ronald BreslowJournal of the American Chemical Society|August 4, 2005
Oxaziridinium salts as hydrophobic epoxidation reagents: remarkable hydrophobically-directed selectivity in olefin epoxidationMark R Biscoe, Ronald BreslowOrganic Letters|March 20, 2009
Selective monoarylation of acetate esters and aryl methyl ketones using aryl chloridesMark R Biscoe, Stephen L BuchwaldSynlett : Accounts and Rapid Communications in Synthetic Organic Chemistry|May 4, 2013
The Use of Tertiary Alkylmagnesium Nucleophiles in Ni-Catalyzed Cross-Coupling ReactionsAmruta Joshi-Pangu, Mark R BiscoeOrganic Letters|November 5, 2004
Requirements for selective hydrophobic acceleration in the reduction of ketonesMark R Biscoe, Christopher Uyeda, Ronald BreslowNature Reviews. Chemistry|April 19, 2021
Stereoselectivity in Pd-catalysed cross-coupling reactions of enantioenriched nucleophilesXinghua Ma, Benjamin Murray, Mark R BiscoeOrganic Letters|February 12, 2011
Nickel-catalyzed Negishi cross-coupling reactions of secondary alkylzinc halides and aryl iodidesAmruta Joshi-Pangu, Madhu Ganesh, Mark R BiscoeChemical Science|September 22, 2015
Configurationally Stable, Enantioenriched Organometallic Nucleophiles in Stereospecific Pd-Catalyzed Cross-Coupling Reactions: An Alternative Approach to Asymmetric SynthesisChao-Yuan Wang, Joseph Derosaa, Mark R BiscoeJournal of the American Chemical Society|May 11, 2011
Nickel-catalyzed Kumada cross-coupling reactions of tertiary alkylmagnesium halides and aryl bromides/triflatesAmruta Joshi-Pangu, Chao-Yuan Wang, Mark R BiscoePageof 3