期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 352, 期 4, 页码 632-636出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200900775
关键词
amidation; copper; 1-methylindoles; 2-phenylpyridines; regioselectivity
资金
- Canada Research Chair (Tier I) foundation
- NESERC
- McGill University
Copper(I) bromide-catalyzed amidation of 2-arylpyridine derivatives and 1-methylindoles with a variety of amides was achieved by employing tert-butyl peroxide (TBP) as oxidant. Aryl halides could be tolerated under the reaction conditions. Neither a special ligand nor a base was required for this amidation process.
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