textjournal article
Unexpected Domino Reaction via Pd-Catalyzed Sonogashira Coupling of Benzimidoyl Chlorides with 1,6-Enynes and Cyclization To Synthesize Quinoline Derivatives
Abstract
A domino reaction via palladium-catalyzed Sonogashira coupling of benzimidoyl chlorides with 1,6-enynes and then cyclization to form quinoline derivatives has been developed. The reaction conditions and the scope of the process are examined, and a plausible mechanism is proposed. The procedure is simple, rapid, and general, and the substrates are readily available- Text
- Journal contribution
- Biophysics
- Biochemistry
- Medicine
- Molecular Biology
- Sociology
- Infectious Diseases
- Enyne
- reaction conditions
- benzimidoyl chlorides
- Cyclization
- Synthesize Quinoline DerivativesA domino reaction
- Sonogashira
- enyne
- form quinoline derivatives
- cyclization
- mechanism
- Benzimidoyl Chlorides
- scope
- Unexpected Domino Reaction
- substrate
- procedure