Catalytic Cycloisomerization-Fluorination Sequence of N-Propargyl Amides by Iodoarene/HF⋅Pyridine/Selectfluor Systems.

Autor: Asari, Naoki, Takemoto, Yusuke, Shinomoto, Yukino, Yagyu, Takuma, Yoshimura, Akira, Zhdankin, Viktor V., Saito, Akio
Předmět:
Zdroj: Asian Journal of Organic Chemistry; Nov2016, Vol. 5 Issue 11, p1314-1317, 4p
Abstrakt: As a first example of metal-free and catalytic fluorinative transformations of alkynes, we developed a cycloisomerization-fluorination sequence of N-propargyl amides catalyzed by an iodine(III) species. The iodine(III) catalyst is in situ generated from iodoarene as a precatalyst with Selectfluor as a fluorinating oxidant in the presence of HF⋅pyridine. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index