14073-22-4Relevant articles and documents
Sustainable conjugate addition of indoles catalyzed by acidic ionic liquid immobilized on silica
Hagiwara, Hisahiro,Sekifuji, Masayoshi,Hoshi, Takashi,Suzuki, Toshio,Quanxi, Bao,Qiao, Kun,Yokoyama, Chiaki
, p. 608 - 610 (2008)
A new protocol for 1,4-conjugate addition of indoles to vinyl ketones has been developed, employing Lewis acidic ionic liquid immobilized on silica, ILIS-SO2Cl, as a catalyst, which exhibited an efficient, mild and recyclable nature. The reacti
Boron-Catalyzed Dehydrative Friedel-Crafts Alkylation of Arenes Using β-Hydroxyl Ketone as MVK Precursor
San, Htet Htet,Huang, Jie,Lei Aye, Seinn,Tang, Xiang-Ying
supporting information, p. 2386 - 2391 (2021/01/04)
Boron-catalyzed environmentally benign dehydrative Friedel-Crafts alkylation of indole/pyrrole and aniline derivatives with β-hydroxyl ketones has been developed for the first time. This method provides an efficient and green replacement of toxic and unst
A rapid and highly efficient Michael addition of methoxybenzenes and indoles to α,β-unsaturated ketones using BF3·OEt2 as a catalyst
Swetha,Raghavender Reddy,Madhu Babu,Meshram
supporting information, p. 4427 - 4431 (2017/10/30)
An efficient and general protocol is described for the Michael addition of α,β-unsaturated ketones with electron-rich arenes/indoles to give alkylated arenes/indoles under mild reaction condition at room temperature. Shorter reaction time, convenient and
