Synthesis of 1,4-diazabicyclo[2.2.2]octane

Synthesis of 1,4-diazabicyclo[2.2.2]octane Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1978, Volume: 14, Number: 4, Pages: 452-454 Pages count : 3 DOI: 10.1007/BF00472167

Authors

Shishkin G.V. , Anisimova I.L.

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Double intramolecular cyclization of N,N′-bis(2-chloroethyl)-N-N′-bis(2-cyanoethyl)ethylenediamine leads to 1,4-bis(2-cyanoethyl)-1,4-diazoniabicyclo[2.2.2]octane dichloride, which undergoes decyanoethylation to 1,4-diazabicyclo[2.2.2]octane when it is heated. The structures of the compounds were confirmed by their IR and PMR spectra. © 1978 Plenum Publishing Corporation.

Shishkin G.V. , Anisimova I.L.
Synthesis of 1,4-diazabicyclo[2.2.2]octane
Chemistry of Heterocyclic Compounds. 1978. V.14. N4. P.452-454. DOI: 10.1007/BF00472167 Scopus РИНЦ OpenAlex

Published print:

Apr 1, 1978

Scopus:	2-s2.0-34250281983
Elibrary:	30992613
OpenAlex:	W2013845157

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