Standard
Non-natural 2 : H -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.
In:
RSC Advances, Vol. 9, No. 65, 2019, p. 37901-37905.
Research output: Contribution to journal › Article › peer-review
Harvard
Sakharov, PA, Koronatov, AN
, Khlebnikov, AF, Novikov, MS, Glukharev, AG, Rogacheva, EV, Kraeva, LA
, Sharoyko, VV, Tennikova, TB & Rostovskii, NV 2019, '
Non-natural 2: H -azirine-2-carboxylic acids: An expedient synthesis and antimicrobial activity',
RSC Advances, vol. 9, no. 65, pp. 37901-37905.
https://doi.org/10.1039/c9ra09345a
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 2: H -azirine-2-carboxylic acids: An expedient synthesis and antimicrobial activity.
RSC Advances,
9(65), 37901-37905.
https://doi.org/10.1039/c9ra09345a
Vancouver
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 2 : H -azirine-2-carboxylic acids: An expedient synthesis and antimicrobial activity. In:
RSC Advances. 2019 ; Vol. 9, No. 65. pp. 37901-37905.
BibTeX
@article{fb4a4ae844dc49ee87b849b70076e8ee,
title = "Non-natural 2: H -azirine-2-carboxylic acids: An expedient synthesis and antimicrobial activity",
abstract = "Non-natural 2H-azirine-2-carboxylic acids were obtained in high yields 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.}",
note = "Publisher Copyright: {\textcopyright} 2019 The Royal Society of Chemistry.",
year = "2019",
doi = "10.1039/c9ra09345a",
language = "English",
volume = "9",
pages = "37901--37905",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "65",
}
RIS
TY - JOUR
T1 - Non-natural 2
T2 - H -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.
N1 - Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Non-natural 2H-azirine-2-carboxylic acids were obtained in high yields 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-carboxylic acids were obtained in high yields 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 - http://www.scopus.com/inward/record.url?scp=85075716325&partnerID=8YFLogxK
U2 - 10.1039/c9ra09345a
DO - 10.1039/c9ra09345a
M3 - Article
AN - SCOPUS:85075716325
VL - 9
SP - 37901
EP - 37905
JO - RSC Advances
JF - RSC Advances
SN - 2046-2069
IS - 65
ER -
