New Chiral and Achiral Imines and Bisimines Derived from 2-Phenyl-1H-imidazole-4-carbaldehyde. Synthesis, Structural Studies and Complexation Stability Constants
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F14%3A39897770" target="_blank" >RIV/00216275:25310/14:39897770 - isvavai.cz</a>
Result on the web
<a href="http://onlinelibrary.wiley.com/doi/10.1002/jhet.1692/pdf" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1002/jhet.1692/pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/jhet.1692" target="_blank" >10.1002/jhet.1692</a>
Alternative languages
Result language
angličtina
Original language name
New Chiral and Achiral Imines and Bisimines Derived from 2-Phenyl-1H-imidazole-4-carbaldehyde. Synthesis, Structural Studies and Complexation Stability Constants
Original language description
2-Phenyl-1H-imidazole-4-carbaldehyde was condensed with achiral and chiral amines or 1,2-diamines. Sixteen condensation products, especially chiral imines and bisimines, were prepared in the 45 to 99 % of yields and characterized. Stability constants ofCu(II) complexes of selected prepared imines/bisimines were determined.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Heterocyclic Chemistry
ISSN
0022-152X
e-ISSN
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Volume of the periodical
51
Issue of the periodical within the volume
3
Country of publishing house
US - UNITED STATES
Number of pages
7
Pages from-to
695-701
UT code for WoS article
000337560000024
EID of the result in the Scopus database
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