Abstract
A strategy for the β-sp3 functionalisation of cyclic amines is described. Regioselective conversion of protected amines to enecarbamates is achieved through electrochemical oxidation; these intermediates can be derivatised by functionalised alkyl halides under photoredox catalysis. The potential of the methods is highlighted by direct growth of a DCP2B-binding fragment. This journal is
Cite
CITATION STYLE
Trindade, A. F., Faulkner, E. L., Leach, A. G., Nelson, A., & Marsden, S. P. (2020). Fragment-oriented synthesis: β-elaboration of cyclic amine fragments using enecarbamates as platform intermediates. Chemical Communications, 56(62), 8802–8805. https://doi.org/10.1039/d0cc03934a
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.