Pyridine-boryl radical mediated synthesis of quinolines via α-amino radical formation and intramolecular alkenyl sulfone trapping | Synapse
April 12, 2026Open Access
Pyridine-boryl radical mediated synthesis of quinolines via α-amino radical formation and intramolecular alkenyl sulfone trapping
Key Points
The aim is to explore the synthesis of quinolines through the mediation of pyridine-boryl radicals and α-amino radicals.
Utilized pyridine-boryl radicals to form α-amino radicals from imines.
Conducted a 6-endo-trig intramolecular trapping with alkenyl sulfones.
Performed reactions under mild conditions to evaluate product formation.
Successfully synthesized quinolines from the reaction of pyridine-boryl radicals.
Achieved formation of α-amino radicals leading to effective quinoline formation.
Confirmed the method's efficacy under mild reaction conditions.
Abstract
Pyridine–boryl radicals trigger α-amino radical formation from imines, enabling a 6- endo-trig intramolecular trapping with alkenyl sulfones to deliver quinolines under mild conditions.
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Cite This Study
Valderrama-Callejón et al. (Thu,) studied this question.