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Chiral 1,4‐bensodiazepines. V. ‐ synthesis and properties of 1,4‐benzodiazepin‐2‐ones containing α‐amino acids as a part of the 1,4‐diazepine ring
37
Citations
9
References
1973
Year
Cyclization RateV. ‐ Synthesisα‐Amino AcidsScheme 1Natural SciencesDrug DiscoveryDiversity-oriented SynthesisMedicineChiral 1,4‐BensodiazepinesOrganic ChemistryStereoselective SynthesisChemistryAbstract Chiral 1,4‐Benzodiazepin‐2‐onesHeterocycle ChemistryPharmacologyEnantioselective SynthesisBiomolecular Engineering
Abstract Chiral 1,4‐benzodiazepin‐2‐ones XIII‐XXIIII (Scheme 1) were prepared starting from N ‐protected α‐amino acids and 2‐amino‐5chlorobenzeophenone; the intermediates I‐XII were isolated and identified. Spectroscopie propertiec of these componds are discussed (ir, nmr); their optical stability, as well as the cyclization rate for XII‐XIII in buffer solution have been determined.
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