Our recent work on #organoautocatalyzed transamination metathesis is featured on the #FrontCover of #AngewandteChemie! Congrats to Volker, Florian, Jonas!🎉 @nat.fau.de

#chemsky #organoautocatalysis #transamination

onlinelibrary.wiley.com/doi/10.1002/...
onlinelibrary.wiley.com/doi/10.1002/...

Development of an Organoautocatalyzed Double σ‐Bond C(sp2)‐N Transamination Metathesis Reaction Organoautocatalyzed transamination metathesis of cyclic tertiary amines is disclosed as a high-yielding, scalable reaction that proceeds under mild, catalyst-free conditions. It operates via a multi-....

Happy to share the final version of our paper! We report #waste-reducing, #cost-efficient synthesis of N-substituted #dihydropyridines. No catalysts or harsh reagents needed! #Organoautocatalysis #Transamination #GreenChem #AngewChem

#ChemSky #AcademicSky

onlinelibrary.wiley.com/doi/10.1002/...

Excited to share our latest paper in #AngewChem! We report an organoautocatalyzed #transamination #metathesis of two C(sp²)–N bonds in cyclic amines - no external catalyst, just an in situ-formed organoautocatalyst doing all the work! #ChemSky #AcademicSky onlinelibrary.wiley.com/doi/10.1002/...