![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Abstract
An efficient aromatic thiocyanation of 1,3,5-trisubstituted pyrazolines occurred regioselectively at the para position of N-benzene rings using ammonium thiocyanate as a thiocyanation reagent and oxone as an oxidant.
ACKNOWLEDGMENT
Project 20572040 was supported by the National Natural Science Foundation of China.
Notes
a 1,3,5-Trisubstituted pyrazoles.
b Overoxidized by oxone; no product was formed.