Palladium N-heterocyclic-carbene-catalyzed ortho-arylation of benzaldehyde derivatives
✍ Scribed by Öznur Dogan; Nevin Gürbüz; İsmail Özdemir; Bekir Çetinkaya
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 99 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20479
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✦ Synopsis
Abstract
New, sterically demanding 1,3‐dialkylbenzimidazolium salts (2a–c) as N‐heterocyclic‐carbene precursors have been synthesized and characterized. The ortho position of aromatic aldehydes was directly and selectively arylated with aryl chlorides in the presence of a catalytic system prepared in situ from Pd(OAc)~2~, 1,3‐dialkylbenzimidazolium chlorides (2a–c), and Cs~2~CO~3~. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:569–574, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20479
📜 SIMILAR VOLUMES
## Abstract magnified image Novel functionalized 1,3‐dialkylimidazolinium salts (LHCl) as NHC precursors have been prepared and successfully applied in palladium‐catalyzed arylation of benzaldehydes. The ortho position of aromatic aldehydes was directly and selectively arylated with aryl chlorides
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