1,2-Disubstituted Hexahydro-1H-benzo[d]imidazoles: Synthesis, Characterization and Stability.

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F10%3A39881348" target="_blank" >RIV/00216275:25310/10:39881348 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

1,2-Disubstituted Hexahydro-1H-benzo[d]imidazoles: Synthesis, Characterization and Stability.

Original language description

Starting from commercially available (hetero)aromatic nitriles and (1R,2R)-cyclohexane-1,2-diamine, nine NH-imidazolines (hexahydro-1H-benzo[d]imidazoles) were synthesized in good yields. The molecular structures of three imidazolines were confirmed by X-ray analysis. N Benzylation afforded some of the desired N-benzyl imidazolines, but was incompatible with imidazolines that possessed strong electron accepting heteroaromatic groups at C2. In the latter cases, the products decomposed during column chromatography to form N,N'-disubstituted cyclohexane-1,2-diamines

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2010

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Synthesis : Journal of Synthetic Organic Chemistry

ISSN

0039-7881

e-ISSN

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Volume of the periodical

neuveden

Issue of the periodical within the volume

22

Country of publishing house

DE - GERMANY

Number of pages

7

Pages from-to

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UT code for WoS article

000284533700021

EID of the result in the Scopus database

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