Beijing National Laboratory for Molecule Sciences (BNLMS), CAS Key Laboratory for Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.
Org Lett. 2013 Nov 15;15(22):5702-5. doi: 10.1021/ol402726d. Epub 2013 Oct 24.
A simple, efficient, and highly atom economic haloamidation of simple alkenes has been developed, using AgBF4 or InBr3/AgBF4 (1:3) as catalyst and N-halophthalimide as both nitrogen and halogen source. A broad range of olefins can be applied to afford vicinal haloamines in good yields and with high regioselectivity and diastereoselectivity.
发展了一种简单、高效、高原子经济性的简单烯烃的偕卤酰胺化反应,使用 AgBF4 或 InBr3/AgBF4(1:3)作为催化剂,N-卤代邻苯二甲酰亚胺作为氮源和卤素源。该反应具有广泛的底物适用性,可以高区域选择性和立体选择性地得到偕二卤代胺,产率良好。