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Journal articles
One-pot synthesis of tertiary alkyl fluorides from methyl oxalates by radical deoxyfluorination under photoredox catalysis
Abstract : Tertiary alkyl fluorides have been prepared from methyl oxalates derived from tertiary alcohols by a sequential one-pot hydrolysis/photoredox catalyzed radical deoxyfluorination sequence. The reaction operates under mild conditions and tolerates a wide range of functional groups. This method provides an alternative approach to ionic deoxyfluorination transformations for the incorporation of Carbone–Fluorine quaternary centers into organic molecules.
https://hal-normandie-univ.archives-ouvertes.fr/hal-02024481
Contributor : Madeleine Roux-Merlin Connect in order to contact the contributor
Submitted on : Tuesday, February 19, 2019 - 11:09:03 AM
Last modification on : Tuesday, October 19, 2021 - 11:34:47 PM
Contributor : Madeleine Roux-Merlin Connect in order to contact the contributor
Submitted on : Tuesday, February 19, 2019 - 11:09:03 AM
Last modification on : Tuesday, October 19, 2021 - 11:34:47 PM
