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Conformational stabilization of isatin Schiff bases -biologically active chemical probes. / Smirnov, Andrey S.; Nikolaev, Dmitriy N.; Gurzhiy, Vlad V.; Smirnov, Sergey N.; Suslonov, Vitaliy S.; Garabadzhiu, Alexander V.; Davidovich, Pavel B.

в: RSC Advances, Том 7, № 17, 2017, стр. 10070-10073.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Smirnov, AS, Nikolaev, DN, Gurzhiy, VV, Smirnov, SN, Suslonov, VS, Garabadzhiu, AV & Davidovich, PB 2017, 'Conformational stabilization of isatin Schiff bases -biologically active chemical probes', RSC Advances, Том. 7, № 17, стр. 10070-10073. https://doi.org/10.1039/c6ra26779c, https://doi.org/10.1039/C6RA26779C

APA

Smirnov, A. S., Nikolaev, D. N., Gurzhiy, V. V., Smirnov, S. N., Suslonov, V. S., Garabadzhiu, A. V., & Davidovich, P. B. (2017). Conformational stabilization of isatin Schiff bases -biologically active chemical probes. RSC Advances, 7(17), 10070-10073. https://doi.org/10.1039/c6ra26779c, https://doi.org/10.1039/C6RA26779C

Vancouver

Author

Smirnov, Andrey S. ; Nikolaev, Dmitriy N. ; Gurzhiy, Vlad V. ; Smirnov, Sergey N. ; Suslonov, Vitaliy S. ; Garabadzhiu, Alexander V. ; Davidovich, Pavel B. / Conformational stabilization of isatin Schiff bases -biologically active chemical probes. в: RSC Advances. 2017 ; Том 7, № 17. стр. 10070-10073.

BibTeX

@article{47a24a061c774985a978c9f16a375d41,
title = "Conformational stabilization of isatin Schiff bases -biologically active chemical probes",
abstract = "Isatin Schiff base derivatives have a wide range of biological effects. Unfortunately, these compounds possess a serious topological shortcoming: the conformational E Z interconversion. Two ways of conformation stabilization are reported here: complexation with metals that stabilize the E-conformer and substitution in the 4th position of the isatin core stabilizing the Z-form.",
author = "Smirnov, {Andrey S.} and Nikolaev, {Dmitriy N.} and Gurzhiy, {Vlad V.} and Smirnov, {Sergey N.} and Suslonov, {Vitaliy S.} and Garabadzhiu, {Alexander V.} and Davidovich, {Pavel B.}",
year = "2017",
doi = "10.1039/c6ra26779c",
language = "English",
volume = "7",
pages = "10070--10073",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "17",

}

RIS

TY - JOUR

T1 - Conformational stabilization of isatin Schiff bases -biologically active chemical probes

AU - Smirnov, Andrey S.

AU - Nikolaev, Dmitriy N.

AU - Gurzhiy, Vlad V.

AU - Smirnov, Sergey N.

AU - Suslonov, Vitaliy S.

AU - Garabadzhiu, Alexander V.

AU - Davidovich, Pavel B.

PY - 2017

Y1 - 2017

N2 - Isatin Schiff base derivatives have a wide range of biological effects. Unfortunately, these compounds possess a serious topological shortcoming: the conformational E Z interconversion. Two ways of conformation stabilization are reported here: complexation with metals that stabilize the E-conformer and substitution in the 4th position of the isatin core stabilizing the Z-form.

AB - Isatin Schiff base derivatives have a wide range of biological effects. Unfortunately, these compounds possess a serious topological shortcoming: the conformational E Z interconversion. Two ways of conformation stabilization are reported here: complexation with metals that stabilize the E-conformer and substitution in the 4th position of the isatin core stabilizing the Z-form.

UR - http://www.scopus.com/inward/record.url?scp=85011982426&partnerID=8YFLogxK

U2 - 10.1039/c6ra26779c

DO - 10.1039/c6ra26779c

M3 - Article

AN - SCOPUS:85011982426

VL - 7

SP - 10070

EP - 10073

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

IS - 17

ER -

ID: 9151661