Abstract
Several ligands were designed to promote transition-metal-free cross-coupling reactions of aryl halides with benzene derivatives. Among the systems probed, quinoline-1-amino-2-carboxylic acid was found to serve as an excellent catalyst for cross-coupling between aryl halides and unactivated benzene. Reactions using this inexpensive catalytic system displayed a high functional group tolerance as well as excellent chemoselectivities.
Original language | English (US) |
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Pages (from-to) | 3556-3559 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 13 |
Issue number | 14 |
DOIs | |
State | Published - Jul 15 2011 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry