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Transallenation of 1,3‐Bis(dialkylamino)‐1,3‐diethoxyallenes with Disubstituted Malonyl Chlorides
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1984
Year
Medicinal ChemistryEngineeringNatural Sciences1,1-Allenedicarboxamides 3Organic ChemistryStereoselective SynthesisChemistryGeneral Synthetic RoutePharmacologyMalonamide Dianions 1Synthetic ChemistryBiomolecular EngineeringDisubstituted Malonyl Chlorides
A general synthetic route to 1,1-allenedicarboxamides 3 is transallenation. For this purpose 1,3-bis (dialkylamino) allenes (synthetic equivalents of malonamide dianions 1) are allowed to react with disubstituted malonyl chlorides (synthetic equivalents of 1,1-vinylidene dications 2); R1NR2.
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