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First Direct Reductive Amination of Mucochloric Acid: A Simple and Efficient Method for Preparing Highly Functionalized α,β-Unsaturated γ-Butyrolactams
43
Citations
59
References
2003
Year
Derivative (Chemistry)Bioorganic ChemistryEngineeringBiochemistryEfficient MethodNatural SciencesOrganic ChemistrySame PotDirect Reductive AminationHighly Functionalized αChemistryPharmacologyMucochloric AcidSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
[reaction: see text] The first direct reductive amination of mucochloric acid (1) has been accomplished. Reaction of 1 with various alkyl, aryl, and benzylamines, followed by reduction in the same pot, provides an efficient method of obtaining N-benzyl-3,4-dichloro-1,5-dihydro-pyrrol-2-one and N-aryl (or alkyl)-3,4-dichloro-1,5-dihydro-pyrrol-2-ones.
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