Chemical Communications · 2014 · 39 citations · 37 references
Natural SciencesChemistryCatalysisOrganic ChemistryAddition ReactionsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisOrganic Synthesis[4+2] CycloadditionAza-diels-alder ReactionAzone DerivativesMild Reaction Conditions
Phosphine-catalyzed [4+1] annulation of electron-deficient 1,3-dienes or 1,3-azadienes with maleimides has been successfully developed under very mild conditions, providing a convenient and highly efficient method for constructing 2-azaspiro[4.4]nonenes and 1,7-diazaspiro[4.4]nonenes. This reaction represents the first example of [4+1] cyclization between electron-deficient 4π-conjugated systems and non-allylic phosphorus ylides.
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