A new mode of carbene-catalyzed heteroatom activation and asymmetric reactions is disclosed. The reaction starts with addition of a carbene catalyst to a (benz)imidazole-derived aldimine substrate. Subsequent oxidation and proton transfer lead to the formation of a catalyst-bound triaza-diene as the key intermediate, in which the nitrogen atom at a site remote to the catalyst-substrate bond is activated. This unusual triaza-diene intermediate then undergoes highly enantioselective reactions with activated ketones through a concerted asynchronous pathway, as supported by mechanistic studies and preliminary density function theory calculation.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.202016506DOI Listing

Publication Analysis

Top Keywords

carbene-catalyzed activation
4
activation remote
4
remote nitrogen
4
nitrogen atoms
4
atoms benzimidazole-derived
4
benzimidazole-derived aldimines
4
aldimines enantioselective
4
enantioselective synthesis
4
synthesis heterocycles
4
heterocycles mode
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!