On Differences between Racemic and Enantiomerically Pure Forms of Aziridine-2-carboxamide
ChemInform 2013
Māris Turks, Inese Rijkure, Sergejs Beļakovs, Daina Zicāne, Viktors Kumpiņš, Ērika Bizdēna, A. Meikas, A. Valkna

A straightforward, reproducible and scalable method for the synthesis of both enantiomers of aziridine-2-carboxamide (Leakadine) is described.


Atslēgas vārdi
aziridine derivatives; diastereoselective syntheses, enantioselective syntheses (incl. cis/trans-isomerism); pharmacology, medicinal chemistry, vaccines, serums
DOI
10.1002/chin.201306058
Hipersaite
http://onlinelibrary.wiley.com/doi/10.1002/chin.201306058/abstract

Turks, M., Rijkure, I., Beļakovs, S., Zicāne, D., Kumpiņš, V., Bizdēna, Ē., Meikas, A., Valkna, A. On Differences between Racemic and Enantiomerically Pure Forms of Aziridine-2-carboxamide. ChemInform, 2013, Vol.44, Iss.6, 58.-58.lpp. ISSN 1522-2667. Pieejams: doi:10.1002/chin.201306058

Publikācijas valoda
English (en)
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