Issue 6, 2004
From the journal:

Mendeleev Communications

Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news

Remir G. Kostyanovsky,a   Oleg R. Malyshev,b   Konstantin A. Lyssenko,c   Yuri A. Strelenko,b   Gul'nara K. Kadorkina,a   Vasily R. Kostyanovsky,a   Orudzh G. Nabieva  and  Ivan V. Fedyaninc  

a N.N. Semenov Institute of Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation, ul. Kosygina, 4, Moscow, Russian Federation

b N.D.Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation, Leninsky prospekt, 47, Moscow, Russian Federation

c A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Moscow, Russian Federation, ul. Vavilova, 28, 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.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1070/MC2004v014n06ABEH002083
Article type
Communication
Submitted
01 Nov 2004

Mendeleev Commun., 2004,14, 315-318

Permissions

Request permissions

Stereochemistry of 1,2,4,5-tetraazanorbornanes and diaziridines: exciting history and news

R. G. Kostyanovsky, O. R. Malyshev, K. A. Lyssenko, Y. A. Strelenko, G. K. Kadorkina, V. R. Kostyanovsky, O. G. Nabiev and I. V. Fedyanin, Mendeleev Commun., 2004, 14, 315 DOI: 10.1070/MC2004v014n06ABEH002083

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements