A combination of IPrAuNTf(2) as catalyst in the presence of Selectfluor has been successfully used for the high yielding synthesis of alpha-fluoroenones via 1,3-acyloxy rearrangement of propargyl acetates followed by Csp(2)-F bond formation, likely involving a redox Au(I)/Au(III) catalytic cycle.
在Selectfluor存在下将IPrAu
NTf(2)用作
催化剂的组合已成功用于通过炔
丙基乙酸酯的1,3-酰
氧基重排,然后形成Csp(2)-F键的高产率合成α-
氟烯酮氧化还原Au(I)/ Au(III)催化循环。