1 h 8 min
Stereochemical journey through carbocations and their precursors
Organic Chemistry, Catalysis and seminar by Jérôme Lacour, ENS Paris
Hosted by Collège de France
Wednesday 11:00 Paris (GMT+1)
Recording available
Amphithéâtre Mireille-Delmas-Marty, Site Marcelin-Berthelot
Recording
Abstract
This seminar connects molecular chirality with the reactivity of cations and their precursors. Helical structures based on delocalized triarylcarbenium frameworks provide a platform for tuning electronic and chiroptical properties. A second focus is metal-catalysed decomposition of diazocarbonyl compounds, yielding ylides and elaborated heterocycles. The discussion includes tetrahetero-substituted methanes with unusually persistent configurations and relates their resistance to enantiomerization to carbocation chemistry.
Topics
molecular chiralitycationstriarylcarbenium frameworksHelical structureschiroptical propertiesmetal-catalysed decompositiondiazocarbonyl compoundsylidesenantiomerization