Selectfluor and alcohol-mediated synthesis of bicyclic oxyfluorination compounds by Wagner–Meerwein rearrangement

Herein, we report the first environmentally friendly systematic fluoroalkoxylation reactions in bicyclic systems. New oxyfluorination products were obtained with excellent yields (up to 98%) via Wagner–Meerwein rearrangement using benzonorbornadiene and the chiral natural compound (+)-camphene as bi...

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Bibliographic Details

Published in:	Beilstein Journal of Organic Chemistry
Main Authors:	Ziya Dağalan, Muhammed Hanifi Çelikoğlu, Saffet Çelik, Ramazan Koçak, Bilal Nişancı
Format:	Article
Language:	English
Published:	Beilstein-Institut 2024-07-01
Subjects:	alkoxyfluorine compounds bicyclic alkene oxyfluorination selectfluor wagner–meerwein rearrangement
Online Access:	https://doi.org/10.3762/bjoc.20.129