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HERO ID
5792781
Reference Type
Journal Article
Title
Reactions of 2-hydroxy-5-(1-adamantyl)benzene-1,3-dicarbaldehyde with ethane-1,2-diamine, trans-cyclohexane-1,2-diamine, and N-(2-aminoethyl)ethane-1,2-diamine
Author(s)
Shokova, EA; Kovalev, VV
Year
2008
Is Peer Reviewed?
1
Journal
Russian Journal of General Chemistry
ISSN:
1070-3632
EISSN:
1608-3350
Volume
78
Issue
11
Page Numbers
2082-2093
Language
English
DOI
10.1134/S1070363208110170
Web of Science Id
WOS:000261959400017
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-59849125726&doi=10.1134%2fS1070363208110170&partnerID=40&md5=56f7f0e6ee273e2047938c322c9521bf
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Abstract
Reactions of 2-hydroxy-5-(1-admantyl)benzene-1,3-dicarbaldehyde with ethane-1,2-diamine, transcyclohexane-1,2-diamine, and N-(2-aminoethyl)ethane-1, 2-diamine were studied in strongly dilute solution and under conditions of template synthesis in the presence of H3BO3. The effects of reaction conditions and initial diamine structure on the cyclocondensation process were determined. Selective [3 + 3]-cyclocondensation of 2-hydroxy-5-(1-admantyl)benzene-1,3-dicarbaldehyde with trans-cyclohexane-1,2- diamine and [2 + 2]-cyclization with N-(2-aminoethyl)ethane-1,2-diamine were performed in chloroform in the presence of H3BO3. The first representative of adamantylcalixsalens was synthesized. © 2008 MAIK Nauka.
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