Publication | Closed Access
Absolute configuration of α-substituted β-lactams from<scp>D</scp>-glyceraldehyde acetonide
32
Citations
0
References
1986
Year
Enantioselective SynthesisBioorganic ChemistryAbsolute ConfigurationBiochemistryNatural SciencesDiversity-oriented SynthesisGlycobiologyOrganic ChemistryPeptide ScienceActive GlyceraldehydeMolecular RearrangementStereoselective SynthesisMedicineAsymmetric CatalysisSynthetic ChemistrySchiff BasesBiomolecular EngineeringNatural Product Synthesis
3,4-Disubstituted-1-arylazetidin-2-ones can be prepared in an enantiospecific manner by the annelation of Schiff bases from optically active glyceraldehyde acetonide and their stereochemistry determined from n.m.r. studies on lactones prepared from these β-lactams by molecular rearrangement.