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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2003, том 13, выпуск 3, страницы 136–139 (Mi mendc3992)

Эта публикация цитируется в 8 статьях

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

Аннотация: Novel cyclic hydrazines 48 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-ray diffraction analysis.

Язык публикации: английский

DOI: 10.1070/MC2003v013n03ABEH001751



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