Результаты исследований: Вклад в журнал › Статья › Рецензирование
Результаты исследований: Вклад в журнал › Статья › Рецензирование
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TY - JOUR
T1 - Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions
AU - Al-Ithawi, W.
AU - Rammohan, A.
AU - Egorov, I.
AU - Nikonov, I.
AU - Kovalev, I.
AU - Kopchuk, D.
AU - Zyryanov, G.
AU - Chupakhin, O.
N1 - The work was carried out with the support of the Russian Science Foundation (RSF grant no. 23-23-00538).
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85178884184
UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001117621900024
U2 - 10.1134/S1070363223140281
DO - 10.1134/S1070363223140281
M3 - Article
VL - 93
SP - S81-S86
JO - Russian Journal of General Chemistry
JF - Russian Journal of General Chemistry
SN - 1070-3632
IS - S1
ER -
ID: 49839422