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Palladium‐Catalyzed C−H Alkenylation of Arenes with Alkynes: Stereoselective Synthesis of Vinyl Chlorides via a 1,4‐Chlorine Migration
Author(s) -
Li Zhen,
Duan WeiLiang
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201808866
Subject(s) - alkyne , chemistry , palladium , stereoselectivity , chlorine , catalysis , ligand (biochemistry) , medicinal chemistry , chlorine atom , organic chemistry , combinatorial chemistry , polymer chemistry , biochemistry , receptor
A directing group‐free, ligand‐promoted palladium‐catalyzed C−H arylation of internal alkynes with simple arenes was developed. Alkenyl chlorides resulting from a 1,4‐chlorine migration or trisubstituted alkenes were produced in moderate to good yields depending on the type of alkyne.
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