Deconstructive fluorination of cyclic amines by carbon-carbon cleavage

Deconstructive functionalizations involving scission of carbon-carbon double bonds are well established. In contrast, unstrained C(sp3)–C(sp3) bond cleavage and functionalization have less precedent. Here we report the use of deconstructive fluorination to access mono- and difluorinated amine derivatives by C(sp3)–C(sp3) bond cleavage in saturated nitrogen heterocycles such as piperidines and pyrrolidines. Silver-mediated ring-opening fluorination using Selectfluor highlights a strategy for cyclic amine functionalization and late-stage skeletal diversification, establishing cyclic amines as synthons for amino alkyl radicals and providing synthetic routes to valuable building blocks.

Source: ScienceNOW - July 12, 2018 Category: Science Authors: Roque, J. B., Kuroda, Y., Göttemann, L. T., Sarpong, R. Tags: Chemistry reports Source Type: news