Chemical Communications · 1998 · 35 citations · 4 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryOrganometallic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsOrganometallic SynthesisAzetidine ChemistryKetone FunctionalizationLactam SynthesisStereoselective SynthesisTrimethylamine N-oxide Formationβ-Lactam Antibiotics
Aziridinyl enones can be converted in good yield into π-allyltricarbonyliron lactam complexes bearing ketone functionality in the side chain; addition of a variety of nucleophiles into the side chains of these complexes proceeds in good yield and excellent (>95%) de to afford secondary and tertiary alcohols which on treatment with trimethylamine N-oxide form the corresponding β-lactams in good yield.
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James A. Dale, Harry S. Mosher · Journal of the American Chemical Society · 1973 · 2.6K citations
Rudolf Aumann, K. Fröhlich, Horst Ring · Angewandte Chemie International Edition in English · 1974 · 50 citations