Journal of Organic Chemistry p. 1504 - 1513 (1992)
Update date:2022-08-04
Topics:
Uno, Hidemitsu
Okada, Shin-ichiro
Ono, Tetsushi
Shiraishi, Yasukazu
Suzuki, Hitomi
In the presence of BF3*OEt2, (perfluoroalkyl)lithiums generated in situ from the reaction of primary perfluoroalkyl iodides and MeLi-LiBr reacted with imines, azines, and nitrones to afford perfluoroalkylated nitrogen-containing compounds in moderate to good yields.This method was successfully applied to the preparation of a (perfluoroalkyl)glycine and optically active perfluoroalkylated amines.
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