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

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Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions. / Al-Ithawi, W.; Rammohan, A.; Egorov, I. et al.
In: Russian Journal of General Chemistry, Vol. 93, No. S1, 2023, p. S81-S86.

Research output: Contribution to journal › Article › peer-review

BibTeX

@article{f8ef266eed964f38bd37427dcbeac013,

title = "Condensation of Amino-thia- and Oxazoles with Indole and 4-Nitrobenzaldehyde under Mechanoactivation Conditions",

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. {\textcopyright} 2023, Pleiades Publishing, Ltd.",

author = "W. Al-Ithawi and A. Rammohan and I. Egorov and I. Nikonov and I. Kovalev and D. Kopchuk and G. Zyryanov and O. Chupakhin",

note = "The work was carried out with the support of the Russian Science Foundation (RSF grant no. 23-23-00538).",

year = "2023",

doi = "10.1134/S1070363223140281",

language = "English",

volume = "93",

pages = "S81--S86",

journal = "Russian Journal of General Chemistry",

issn = "1070-3632",

publisher = "Maik Nauka-Interperiodica Publishing",

number = "S1",

}

RIS

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