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Metathesis of Azomethine Imines in Reaction of 6-aryl-1,5-Diazabicyclo[3.1.0]Hexanes with (Het)Arylidenemalononitriles Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2013, Volume: 23, Number: 1, Pages: 34-36 Pages count : 3 DOI: 10.1016/j.mencom.2013.01.012
Authors Pleshchev Mikhail I. 1 , Petukhova Vera Yu. 1 , Kuznetsov Vladimir V. 1 , Khakimov Dmitriy V. 1 , Pivina Tatyana S. 1 , Struchkova Marina I. 1 , Nelyubina Yulia V. 2 , Makhova Nina N. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Abstract: Ring opening in 6-aryl-1,5-diazabicyclo[3.1.0]hexanes gives cyclic azomethine imines which are prone to exchange of arylidene moiety with (het)arylidenemalononitriles to form the metathesis products being new azomethine imines. These species were fixed as pyrazolines due to the 1,4-H shift or trapped by dimethyl acetylenedicarboxylate or CS2.
Cite: Pleshchev M.I. , Petukhova V.Y. , Kuznetsov V.V. , Khakimov D.V. , Pivina T.S. , Struchkova M.I. , Nelyubina Y.V. , Makhova N.N.
Metathesis of Azomethine Imines in Reaction of 6-aryl-1,5-Diazabicyclo[3.1.0]Hexanes with (Het)Arylidenemalononitriles
Mendeleev Communications. 2013. V.23. N1. P.34-36. DOI: 10.1016/j.mencom.2013.01.012 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000315320000012
Scopus: 2-s2.0-84873835329
OpenAlex: W2952013955
Citing:
DB Citing
OpenAlex 29
Scopus 27
Web of science 28
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