Unexpected isocyanide-based cascade cycloaddition reaction with methyleneindolinone
Chemical Communications2013Vol. 49(91), pp. 10694–10694
Citations Over TimeTop 10% of 2013 papers
Abstract
An unprecedented cascade reaction of isocyanide and methyleneindolinone has been established, which represents a novel and different reaction mode. This present transformation involves the ring-opening of methyleneindolinone and the construction of two other new rings simultaneously in an atom-economic manner.
Related Papers
- → Recent Progress in Metal-Catalyzed [2+2+2] Cycloaddition Reactions(2021)96 cited
- → Acetylene and Ethylene: Universal C2 Molecular Units in Cycloaddition Reactions(2021)27 cited
- → Addition Reactions: Cycloaddition(2017)1 cited
- → Addition Reactions: Cycloaddition(2019)
- → Addition Reactions: Cycloaddition(2014)