Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones

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Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. / Gein, V. L.; Kazantseva, M. I. ; Varkentin, L. I.; Zamaraeva, T. M.; Yankin, A. N.; Beletskii, E. V.; Novikova, V. V.

в: Russian Journal of General Chemistry, Том 90, № 8, 01.08.2020, стр. 1426-1431.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Author

Gein, V. L. ; Kazantseva, M. I. ; Varkentin, L. I. ; Zamaraeva, T. M. ; Yankin, A. N. ; Beletskii, E. V. ; Novikova, V. V. / Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. в: Russian Journal of General Chemistry. 2020 ; Том 90, № 8. стр. 1426-1431.

BibTeX

@article{a6bc567c02e940a7965712527ac91335,

title = "Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones",

abstract = "Abstract: The reaction of tryptamine with aromatic aldehydes and 4-chlorobenzoylpyruvic acid methyl ester led to the formation of 5-aryl-4-[hydroxy-(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. The resulting compounds were tested for antimicrobial activity.",

keywords = "antimicrobial activity, N,N-dimethyltryptamine heterocyclic analogues, pyrrolidine-2,3-dione derivatives, N-dimethyltryptamine heterocyclic analogues, INHIBITORY-ACTIVITY, pyrrolidine-2, 3-dione derivatives, DERIVATIVES, EFFICIENT, N",

author = "Gein, {V. L.} and Kazantseva, {M. I.} and Varkentin, {L. I.} and Zamaraeva, {T. M.} and Yankin, {A. N.} and Beletskii, {E. V.} and Novikova, {V. V.}",

note = "Gein, V.L., Kazantseva, M.I., Varkentin, L.I. et al. Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. Russ J Gen Chem 90, 1426–1431 (2020). https://doi.org/10.1134/S1070363220080083",

year = "2020",

month = aug,

day = "1",

doi = "10.1134/S1070363220080083",

language = "English",

volume = "90",

pages = "1426--1431",

journal = "Russian Journal of General Chemistry",

issn = "1070-3632",

publisher = "МАИК {"}Наука/Интерпериодика{"}",

number = "8",

}

RIS

TY - JOUR

T1 - Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones

AU - Gein, V. L.

AU - Kazantseva, M. I.

AU - Varkentin, L. I.

AU - Zamaraeva, T. M.

AU - Yankin, A. N.

AU - Beletskii, E. V.

AU - Novikova, V. V.

N1 - Gein, V.L., Kazantseva, M.I., Varkentin, L.I. et al. Synthesis and Antibacterial Activity of 5-Aryl-4-[hydroxy(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. Russ J Gen Chem 90, 1426–1431 (2020). https://doi.org/10.1134/S1070363220080083

PY - 2020/8/1

Y1 - 2020/8/1

N2 - Abstract: The reaction of tryptamine with aromatic aldehydes and 4-chlorobenzoylpyruvic acid methyl ester led to the formation of 5-aryl-4-[hydroxy-(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. The resulting compounds were tested for antimicrobial activity.

AB - Abstract: The reaction of tryptamine with aromatic aldehydes and 4-chlorobenzoylpyruvic acid methyl ester led to the formation of 5-aryl-4-[hydroxy-(4-chlorophenyl)methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. The resulting compounds were tested for antimicrobial activity.

KW - antimicrobial activity

KW - N,N-dimethyltryptamine heterocyclic analogues

KW - pyrrolidine-2,3-dione derivatives

KW - N-dimethyltryptamine heterocyclic analogues

KW - INHIBITORY-ACTIVITY

KW - pyrrolidine-2

KW - 3-dione derivatives

KW - DERIVATIVES

KW - EFFICIENT

KW - N

UR - http://www.scopus.com/inward/record.url?scp=85091038289&partnerID=8YFLogxK

U2 - 10.1134/S1070363220080083

DO - 10.1134/S1070363220080083

M3 - Article

AN - SCOPUS:85091038289

VL - 90

SP - 1426

EP - 1431

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 8

ER -

ID: 70169330