952-43-2Relevant articles and documents
Using fast scanning calorimetry to study solid-state cyclization of dipeptide L-leucyl-L-leucine
Buzyurov, Aleksey V.,Gerasimov, Alexander V.,Gorbatchuk, Valery V.,Safiullina, Aisylu S.,Schick, Christoph,Ziganshin, Marat A.,Ziganshina, Sufia A.
, (2020/08/22)
The possibility of using fast scanning calorimetry (FSC) to study the kinetics of the solid-state cyclization of dipeptide was demonstrated in the present work for the first time. The activation energy and Arrhenius constant of the cyclization of L/
Thermally Induced Self-Assembly and Cyclization of l -Leucyl- l -Leucine in Solid State
Ziganshin, Marat A.,Safiullina, Aisylu S.,Gerasimov, Alexander V.,Ziganshina, Sufia A.,Klimovitskii, Alexander E.,Khayarov, Khasan R.,Gorbatchuk, Valery V.
, p. 8603 - 8610 (2017/09/22)
Thermal treatment of oligopeptides is one of the methods for synthesis of organic nanostructures. However, heating may lead not only to self-assembly of the initial molecules, but also to chemical reactions resulting in the formation of new unexpected nan
Biomimetic epoxidation in aqueous media catalyzed by cyclic dipeptides
Bérubé, Christopher,Voyer, Normand
supporting information, p. 395 - 403 (2016/04/05)
We have developed a practical epoxidation of electron-deficient enones in aqueous media using cyclic dipeptides as bioinspired green catalyst. Optimizing the reaction conditions in a triphasic system led to efficient conditions providing epoxides with good enantioselectivities. Depending on the catalyst substituent chirality, both enantiomers are obtained. The cyclic rigidity impacts significantly the enantioselectivity.
