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CHEMICAL COMMUNICATIONS
Volume -, Issue -, Pages -Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc03151
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We have revealed a Rauhut-Currier reaction of γ-alkyl-substituted allenoate catalyzed by l-valine-derived amide phosphine to generate trisubstituted allenoate, which then undergoes a Diels-Alder reaction with maleimide or DMAD. The reaction achieves the construction of exo-bicyclic succinimide derivatives with three consecutive stereocenters and an exo-carbon-carbon double bond in high stereospecificity and almost quantitative yields.
We have disclosed a Rauhut-Currier reaction of & gamma;-alkyl-substituted allenoate, catalyzed by l-valine-derived amide phosphine, to form trisubstitued allenoate, which was trapped by maleimide or DMAD via the Diels-Alder reaction. Exo-bicyclic succinimide derivatives including three continuous stereocenters with an exo-carbon-carbon double bound were constructed in up to quantitative yields with high stereospecificity. We have disclosed a Rauhut-Currier reaction of & gamma;-alkyl-substituted allenoate, catalyzed by l-valine-derived amide phosphine, to form trisubstitued allenoate, which was trapped by maleimide or DMAD via the Diels-Alder reaction.
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