Lewis acid catalyzed intramolecular halo-arylation of tethered alkenes using N-halosuccinimide (NXS) as the halogen source:: a general method for the synthesis of chromanones, chromans, quinolones, tetrahydroquinolines and tetralins
Lewis acid catalyzed intramolecular halo-arylation of tethered alkenes using N-halosuccinimide (NXS) as the halogen source:: a general method for the synthesis of chromanones, chromans, quinolones, tetrahydroquinolines and tetralins
复制标题
DOI：
10.1016/j.tetlet.2005.09.170
复制
发表时间：
2005-12-05
影响因子：
1.8
通讯作者：
Karmakar, A
中科院分区：
文献类型：
--
作者：
Hajra, S;Maji, B;Karmakar, A
Lewis acid catalyzed intramolecular halo-arylation of tethered alkenes was performed using N-halosuccinimide (NXS) as the halogen source. Among the Lewis acids investigated, Sm(OTf)(3) was found to be the best catalyst. This catalytic process provides a general method for the regio- and stereoselective synthesis of annulated arene heterocycles and carbocycles Such as 2-chromanones, chromans, 2-quinolones, tetrahydroquinolines and tetralins possessing a halo-functionality. (c) 2005 Elsevier Ltd. All rights reserved.
