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Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions

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Заглавие Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions
 
Автор Al-Ithawi, W. K. A.
Rammohan, A.
Egorov, I. N.
Nikonov, I. L.
Kovalev, I. S.
Kopchuk, D. S.
Zyryanov, G. V.
Chupakhin, O. N.
 
Тематика 4-NITROBESALDEHYDE
ADDITION AT THE C=N BOND
ADDITION PRODUCT
AZOLYL-AMINES
INDOLE
SCHIFF BASE
 
Описание Abstract: The reactions of isoxazol-3-amine, thiazol-2-amine, benzo[d]thiazol-2-amine with 4-nitrobenzaldehyde and indole in the absence of a solvent under ball-milling conditions were studied. The reactions proceed through the in situ formation of a Schiff base and subsequent nucleophilic addition of indole at the C=N fragment to form the addition products, α,α-disubstituted azolyl-amines, in yields up to 80%. The structure of the products was proved by physicochemical methods. © 2023, Pleiades Publishing, Ltd.
Russian Science Foundation, RSF: 23-23-00538
The work was carried out with the support of the Russian Science Foundation (RSF grant no. 23-23-00538).
 
Дата 2024-05-23T08:40:06Z
2024-05-23T08:40:06Z
2023
 
Тип Article
Journal article (info:eu-repo/semantics/article)
Published version (info:eu-repo/semantics/publishedVersion)
 
Идентификатор Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions / W. K. A. Al-Ithawi, A. Rammohan, I. N. Egorov [et al.] // Russian Journal of General Chemistry. – 2023. – Vol. 93. – P. S81-S86. DOI: 10.1134/S1070363223140281.
1070-3632
no full text
https://elar.usfeu.ru/handle/123456789/13185
 
Язык en
 
Издатель Pleiades Publishing
 
Источник Russian Journal of General Chemistry