Issue 5, 2003
From the journal:

Mendeleev Communications

Chiral aziridine-trans-2,3-dicarboxylic acid derivatives: exciting history, re-examination and structures

Remir G. Kostyanovsky,*a   Oleg N. Krutius,a   Andrey A. Stankevichb  and  Konstantin A. Lyssenkoc  

* Corresponding authors

a N.N. Semenov Institute of Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation, ul. Kosygina, 4, Moscow, Russian Federation
E-mail: kost@chph.ras.ru

b Higher Chemical College, Russian Academy of Sciences, Moscow, Russian Federation, Miusskaya ploshchad, 9, 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

Chiral aziridines 5, 6 and enamine 7 were synthesised; compounds B, C and D, which were obtained over 100 years ago, were not aziridines; the product described as B was identified with isomeric enamine 7. The crystal structures of aziridines (±)- and (+)-6 were studied.

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Article information

DOI
https://doi.org/10.1070/MC2003v013n05ABEH001806
Article type
Communication
Submitted
27 May 2003

Mendeleev Commun., 2003,13, 223-226

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Chiral aziridine-trans-2,3-dicarboxylic acid derivatives: exciting history, re-examination and structures

R. G. Kostyanovsky, O. N. Krutius, A. A. Stankevich and K. A. Lyssenko, Mendeleev Commun., 2003, 13, 223 DOI: 10.1070/MC2003v013n05ABEH001806

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