Key Laboratory of Natural Pesticide and Chemical Biology, Ministry of Education, South China Agricultural University, Guangzhou 510642, China.
State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, South China Agricultural University, Guangzhou 510642, China.
Molecules. 2018 Dec 14;23(12):3317. doi: 10.3390/molecules23123317.
1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP) was found to be effective for the Bischler indole synthesis under microwave irradiation in the absence of a metal catalyst. Under the catalysis of HFIP, a wide range of α-amino arylacetones were successfully transformed into indole derivatives with moderate to good yields.
1,1,1,3,3,3-六氟-2-丙醇(HFIP)在微波辐射下,无需金属催化剂,即可有效用于 Bischler 吲哚合成。在 HFIP 的催化作用下,各种α-氨基芳基乙酮成功转化为吲哚衍生物,产率中等至良好。