NICKEL-CATALYZED ELECTROCHEMICAL COUPLING OF 2-BROMOTHIOPHENE AND 3-BROMOTHIOPHENE WITH ALKYL AND ALKENYL HALIDES

Citation
M. Durandetti et al., NICKEL-CATALYZED ELECTROCHEMICAL COUPLING OF 2-BROMOTHIOPHENE AND 3-BROMOTHIOPHENE WITH ALKYL AND ALKENYL HALIDES, Tetrahedron letters, 38(50), 1997, pp. 8683-8686
Citations number
15
Journal title
ISSN journal
00404039
Volume
38
Issue
50
Year of publication
1997
Pages
8683 - 8686
Database
ISI
SICI code
0040-4039(1997)38:50<8683:NECO2A>2.0.ZU;2-7
Abstract
2- or 3-bromothiophene are efficiently coupled with activated alkyl ch lorides (alpha-chloroesters, alpha-chloroketones, alpha-chloronitriles ), benzyl chloride or vinyl halides, in a one step electrochemical rea ction, using the sacrificial anode process and catalysis by NiBr2-2,2' -bipyridine (bipy). (C) 1997 Elsevier Science Ltd.