Standard

Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity. / Sakharov, Pavel A. ; Koronatov, Alexander N. ; Khlebnikov, Alexander F. ; Novikov, Mikhail S. ; Glukharev, Artem G. ; Rogacheva, Elizaveta V. ; Kraeva, Liudmila A. ; Sharoyko, Vladimir V. ; Tennikova, Tatiana B. ; Rostovskii, Nikolai V. .

в: RSC Advances, Том 9, № 65, 21.11.2019, стр. 9864–9873.

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

Harvard

Sakharov, PA, Koronatov, AN, Khlebnikov, AF, Novikov, MS, Glukharev, AG, Rogacheva, EV, Kraeva, LA, Sharoyko, VV, Tennikova, TB & Rostovskii, NV 2019, 'Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity', RSC Advances, Том. 9, № 65, стр. 9864–9873.

APA

Sakharov, P. A., Koronatov, A. N., Khlebnikov, A. F., Novikov, M. S., Glukharev, A. G., Rogacheva, E. V., Kraeva, L. A., Sharoyko, V. V., Tennikova, T. B., & Rostovskii, N. V. (2019). Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity. RSC Advances, 9(65), 9864–9873.

Vancouver

Sakharov PA, Koronatov AN, Khlebnikov AF, Novikov MS, Glukharev AG, Rogacheva EV и пр. Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity. RSC Advances. 2019 Нояб. 21;9(65):9864–9873.

Author

Sakharov, Pavel A. ; Koronatov, Alexander N. ; Khlebnikov, Alexander F. ; Novikov, Mikhail S. ; Glukharev, Artem G. ; Rogacheva, Elizaveta V. ; Kraeva, Liudmila A. ; Sharoyko, Vladimir V. ; Tennikova, Tatiana B. ; Rostovskii, Nikolai V. . / Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity. в: RSC Advances. 2019 ; Том 9, № 65. стр. 9864–9873.

BibTeX

@article{4d4a96c7d3fc483c92ae179bbfe08271,
title = "Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity",
abstract = "Non-natural 2H-azirine-2-carboxylicacidswereobtainedinhighyields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3-heteroaryl-substituted acids are stable during prolonged storage, exhibit antibacterial activity against ESKAPE pathogens and show a low level of cytotoxicity.",
author = "Sakharov, {Pavel A.} and Koronatov, {Alexander N.} and Khlebnikov, {Alexander F.} and Novikov, {Mikhail S.} and Glukharev, {Artem G.} and Rogacheva, {Elizaveta V.} and Kraeva, {Liudmila A.} and Sharoyko, {Vladimir V.} and Tennikova, {Tatiana B.} and Rostovskii, {Nikolai V.}",
year = "2019",
month = nov,
day = "21",
language = "English",
volume = "9",
pages = "9864–9873",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "65",

}

RIS

TY - JOUR

T1 - Non-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activity

AU - Sakharov, Pavel A.

AU - Koronatov, Alexander N.

AU - Khlebnikov, Alexander F.

AU - Novikov, Mikhail S.

AU - Glukharev, Artem G.

AU - Rogacheva, Elizaveta V.

AU - Kraeva, Liudmila A.

AU - Sharoyko, Vladimir V.

AU - Tennikova, Tatiana B.

AU - Rostovskii, Nikolai V.

PY - 2019/11/21

Y1 - 2019/11/21

N2 - Non-natural 2H-azirine-2-carboxylicacidswereobtainedinhighyields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3-heteroaryl-substituted acids are stable during prolonged storage, exhibit antibacterial activity against ESKAPE pathogens and show a low level of cytotoxicity.

AB - Non-natural 2H-azirine-2-carboxylicacidswereobtainedinhighyields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3-heteroaryl-substituted acids are stable during prolonged storage, exhibit antibacterial activity against ESKAPE pathogens and show a low level of cytotoxicity.

UR - https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra09345a#!divAbstract

M3 - Article

VL - 9

SP - 9864

EP - 9873

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

IS - 65

ER -

ID: 49169488