64605-74-9Relevant academic research and scientific papers
Catalytic regioselective synthesis of structurally diverse indene derivatives from N-benzylic sulfonamides and disubstituted alkynes
Liu, Cong-Rong,Yang, Fu-Lai,Jin, Yi-Zhou,Ma, Xian-Tao,Cheng, Dao-Juan,Li, Nan,Tian, Shi-Kai
supporting information; experimental part, p. 3832 - 3835 (2010/11/17)
An unprecedented protocol has been developed for the regioselective synthesis of structurally diverse indene derivatives from readily accessible N-benzylic sulfonamides and disubstituted alkynes through FeCl 3-catalyzed cleavage of sp3 carbon-nitrogen bonds to generate benzyl cation intermediates. In the presence of 10 mol % of FeCl 3, a broad range of N-benzylic sulfonamides smoothly react with internal alkynes, alkynylcarbonyl compounds, alkynyl chalcogenides, or alkynyl halides to afford various functionalized indene derivatives with extremely high regioselectivity.
