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α‐Aminoaldehydes from Enamines and Chloramine‐T
17
Citations
6
References
1979
Year
BiosynthesisBioorganic ChemistryEngineeringBiochemistryAldehyde DehydrogenaseNatural SciencesChloramine T.Organic ChemistryStereoselective SynthesisPharmacologyFacile EntryEnantioselective Synthesisα-Amino Aldehyde GroupNatural Product Synthesis
A facile entry to the α-amino aldehyde group, which occurs in antibiotic sugars and other natural products, is provided by the reaction of enamines (1) with chloramine T. The conditions are very mild and the yields are high.
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