Radical fluorination powered expedient synthesis of 3-fluorobicyclo[1.1.1]pentan-1-amine†
Abstract
Exploration of novel chemical space, a modern trend in medicinal chemistry, is heavily reliant on synthetic access to new and interesting building blocks. In this direction, the following work describes an expedient synthesis of one such moiety, 3-fluorobicyclo[1.1.1]pentan-1-amine, by employing radical fluorination.
- This article is part of the themed collection: Contemporary Synthetic Chemistry in Drug Discovery