Premium
Thioesters as Bifunctional Reagents for 2‐Naphthylamine Sulfuracylation
Author(s) -
Xiao Fuhong,
Yuan Shanshan,
Wang Dahan,
Liu Saiwen,
Huang Huawen,
Deng GuoJun
Publication year - 2019
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201900301
Subject(s) - chemistry , bifunctional , chemoselectivity , reagent , substrate (aquarium) , scope (computer science) , combinatorial chemistry , functional group , organic chemistry , catalysis , computer science , oceanography , polymer , programming language , geology
An efficient and convenient strategy for the preparation of diaryl sulfides via a Fe‐promoted direct sulfuracylation of 2‐naphthylamine using thioesters as bifunctional reagents is described. This synthetic strategy features high chemoselectivity, good substrate scope and functional group tolerance.