Highly regio- and stereoselective trans-iodofluorination of ynamides enabling the synthesis of (E)-α-fluoro-β-iodoenamides
Halogenation
Stereoisomerism
Chemistry Techniques, Synthetic
Amides
01 natural sciences
Catalysis
Iodine
0104 chemical sciences
DOI:
10.1039/c7ob01470h
Publication Date:
2017-08-09T11:33:26Z
AUTHORS (8)
ABSTRACT
A highly regio- and stereoselective <italic>trans</italic>-iodofluorination of <italic>N</italic>-(1-alkynyl)amides with NIS Et<sub>3</sub>N·3HF was achieved, affording (<italic>E</italic>)-α-fluoro-β-iodoenamides in moderate to excellent yields.
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