|
This article is cited in 8 scientific papers (total in 8 papers)
Nitrogen chirality via the sterical veto of N inversion
S. V. Usacheva, G. A. Nikiforovb, Yu. A. Strelenkoc, I. I. Chervina, K. A. Lyssenkod, R. G. Kostyanovskya a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b N.M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
c N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
d A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
Novel cyclic hydrazines 4–8 with sterically hindered (4, 6, 7) or arrested (5, 8) nitrogen inversion were synthesised; pyrazolydine 5 was separated into enantiomers by chiral chromatography; the crystal structures of salts 5a and 5b were studied by X-raydiffraction analysis.
Citation:
S. V. Usachev, G. A. Nikiforov, Yu. A. Strelenko, I. I. Chervin, K. A. Lyssenko, R. G. Kostyanovsky, “Nitrogen chirality via the sterical veto of N inversion”, Mendeleev Commun., 13:3 (2003), 136–139
Linking options:
https://www.mathnet.ru/eng/mendc3992 https://www.mathnet.ru/eng/mendc/v13/i3/p136
|
|