Nucleophilic Addition of Benzimidazoles to Alkynyl Bromides/Palladium-Catalyzed Intramolecular C–H Vinylation: Synthesis of Benzo[4,5]imidazo[2,1-a]isoquinolines
The Journal of Organic Chemistry2012Vol. 78(3), pp. 1242–1248
Citations Over TimeTop 11% of 2012 papers
Abstract
An efficient "one-pot" route for the synthesis of benzo[4,5]imidazo[2,1-a] isoquinolines has been developed via nucleophilic addition of 2-aryl benzimidazoles to alkynyl bromides and subsequent palladium-catalyzed intramolecular C-H vinylation.
Related Papers
- → Preparation of organo palladium sols from palladium complexes in various alcohols(1994)32 cited
- → The constitution of cerium-palladium alloys containing 50–100% palladium(1967)48 cited
- → Allyl(β‐diketonato)palladium(II) complexes as precursors for palladium films(1994)36 cited
- → Reduction of palladium(II) monoglycinate complexes at rotating disc palladium electrode in acid media(2010)1 cited
- Rapid Determination of Palladium in Palladium-Nickel and Palladium-Cobalt Plating Bath(2003)