137577-94-7Relevant academic research and scientific papers
Atom-efficient synthesis of 2,6-diazacyclophane compounds through alcoholysis/reduction of 3-nitroarylmethylene-2,5-piperazinediones
González, Juan Francisco,de la Cuesta, Elena,Avenda?o, Carmen
, p. 2762 - 2771 (2008)
Readily available cyclic dehydrodipeptides are convenient starting materials for atom-efficient synthesis of different compounds. A one-pot ring-opening/alcoholysis/hydrolysis process with 3-nitroarylmethylene-2,5-piperazinediones yielded N-3-nitroarylpyr
From cyclic dehydrodipeptides to uncommon acyclic peptide mimetics
González, Juan Francisco,de la Cuesta, Elena,Avenda?o, Carmen
, p. 6711 - 6714 (2007/10/03)
1-Acetyl-3-arylmethylene-2,5-piperazinediones gave N-3-arylpyruvylamino esters by acid-promoted alcoholysis under thermal conditions or microwave irradiation. Compounds obtained from 1-acetyl-3-(o-nitro)arylmethylene-2,5-piperazinediones gave, after reduc
