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Mendeleev Communications, 1996, Volume 6, Issue 3, Pages 106–107
DOI: https://doi.org/10.1070/MC1996v006n03ABEH000601
(Mi mendc4935)
 

This article is cited in 13 scientific papers (total in 13 papers)

1,2-Di-tert-butyldiaziridine

R. G. Kostyanovskya, V. A. Korneeva, I. I. Chervina, V. N. Voznesenskya, Yu. V. Puzanova, P. Rademacherb

a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b Institute of Organic Chemistry, University of Essen, Germany
Abstract: 1,2-Di-tert-butyldiaziridine 1 has been synthesized for the first time and its 1H and 13C NMR spectra studied in comparison with model diaziridines 810. Its photoelectron and mass spectra have been measured and its structure optimized by semiempirical and ab initio calculations; considerable steric deformation of the CH2 ring fragment and mutual approach of tert-butyl groups is shown.
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Document Type: Article
Language: English


Citation: R. G. Kostyanovsky, V. A. Korneev, I. I. Chervin, V. N. Voznesensky, Yu. V. Puzanov, P. Rademacher, “1,2-Di-tert-butyldiaziridine”, Mendeleev Commun., 6:3 (1996), 106–107
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  • This publication is cited in the following 13 articles:
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