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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
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Recording

1 h 8 min

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