Fillery, Shaun M. published the artcileExpeditious Access to Functionalized Tricyclic Pyrrolo-Pyridones via Tandem or Sequential C-N/C-C Bond Formations, Computed Properties of 22483-09-6, the main research area is tricyclic pyrrolopyridone preparation; bromopyridone bromoaniline cyclic ketone Buchwald Hartwig Heck Fischer indole.
The facile synthesis of both saturated and unsaturated tricyclic pyrrolo-pyridones starting from a single readily available, common monocyclic reagent has been developed. An intermol. annulation via a tandem Buchwald-Hartwig/Heck reaction led to the synthesis of β-carbolinones. The analogous semisatd. tricyclic pyrrolo-pyridones were prepared in good to excellent yields by sequential Buchwald-Hartwig and Fischer indole reactions. The methods feature mild reaction conditions and good functional group tolerance.
Organic Letters published new progress about Anilines Role: RCT (Reactant), RACT (Reactant or Reagent) (bromo). 22483-09-6 belongs to class alcohols-buliding-blocks, name is 2,2-Dimethoxyethanamine, and the molecular formula is C4H11NO2, Computed Properties of 22483-09-6.
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