|
This article is cited in 5 scientific papers (total in 5 papers)
Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news
R. G. Kostyanovskya, O. R. Malyshevb, K. A. Lyssenkoc, Yu. A. Strelenkob, G. K. Kadorkinaa, V. R. Kostyanovskya, O. G. Nabieva, I. V. Fedyaninc a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
The enantiomers of asymmetric nitrogen compound 1 have been resolved; a chiral formal meso-form of diaziridine 2 has been obtained; a population of 1,2-cis-form 6a in solution has been found; and the crystal structures of 3–6 have been studied.
Citation:
R. G. Kostyanovsky, O. R. Malyshev, K. A. Lyssenko, Yu. A. Strelenko, G. K. Kadorkina, V. R. Kostyanovsky, O. G. Nabiev, I. V. Fedyanin, “Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news”, Mendeleev Commun., 14:6 (2004), 315–318
Linking options:
https://www.mathnet.ru/eng/mendc3925 https://www.mathnet.ru/eng/mendc/v14/i6/p315
|
|