Microwave-Assisted Synthesis of N-Substituted Maleimide Derivatives as Exogenous Antioxidant Agents

Rammohan, A.; Mallikarjuna Reddy, G.; Raul, Garcia, J.; Zyryanov, G. V.; Sravya, G.; Bakthavatchala Reddy, N.; Yuvaraja, G.; Зырянов, Г. В.

doi:10.1002/jhet.3421

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Поле DC	Значение	Язык
dc.contributor.author	Rammohan, A.	en
dc.contributor.author	Mallikarjuna Reddy, G.	en
dc.contributor.author	Raul, Garcia, J.	en
dc.contributor.author	Zyryanov, G. V.	en
dc.contributor.author	Sravya, G.	en
dc.contributor.author	Bakthavatchala Reddy, N.	en
dc.contributor.author	Yuvaraja, G.	en
dc.contributor.author	Зырянов, Г. В.	ru
dc.date.accessioned	2021-08-31T15:00:26Z	-
dc.date.available	2021-08-31T15:00:26Z	-
dc.date.issued	2019	-
dc.identifier.citation	Microwave-Assisted Synthesis of N-Substituted Maleimide Derivatives as Exogenous Antioxidant Agents / A. Rammohan, G. Mallikarjuna Reddy, J. Raul Garcia, et al. — DOI 10.1002/jhet.3421 // Journal of Heterocyclic Chemistry. — 2019. — Vol. 56. — Iss. 2. — P. 470-476.	en
dc.identifier.issn	0022152X	-
dc.identifier.other	Final	2
dc.identifier.other	All Open Access, Green	3
dc.identifier.other	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85057838110&doi=10.1002%2fjhet.3421&partnerID=40&md5=8ff8d575739dd92f9c9709299f6915a9
dc.identifier.other	https://elar.urfu.ru/bitstream/10995/76690/1/978-5-7996-2691-4_091.pdf	m
dc.identifier.uri	http://elar.urfu.ru/handle/10995/101897	-
dc.description.abstract	A series of N-substituted maleimide derivatives have been developed via acetic acid-mediated microwave reaction pathway, which was identified as the incomparable method for this maleimide compounds. All the synthesized compounds were tested for antioxidant activity by DPPH and H 2 O 2 methods. Compounds 5h and 5m were displayed with higher antioxidant activity in two methods. The structure–activity relationship demonstrated that the compounds having electron releasing substitutions 5h and 5m generally show beneficial activity than electron capture substitution cores. Thus, compounds 5h and 5m may be useful as an exogenous antioxidant. © 2018 Wiley Periodicals, Inc.	en
dc.format.mimetype	application/pdf	en
dc.language.iso	en	en
dc.publisher	HeteroCorporation	en
dc.rights	info:eu-repo/semantics/openAccess	en
dc.source	J. Heterocycl. Chem.	2
dc.source	Journal of Heterocyclic Chemistry	en
dc.subject	1 [4 (BENZYLIDENEAMINO)PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(2 AMINOBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(2 BROMOBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(2 FLUOROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(2 IODOBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(3 CHLOROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 BROMOBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 CHLOROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 FLUOROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 HYDROXYBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 IODOBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 METHOXYBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 METHYLBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 NITROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1 [4 [(4 TRIFLUOROBENZYLIDENE)AMINO]PHENYL] 1H PYRROLE 2,5 DIONE	en
dc.subject	1,1 DIPHENYL 2 PICRYLHYDRAZYL	en
dc.subject	ACETIC ACID	en
dc.subject	ASCORBIC ACID	en
dc.subject	HYDROGEN PEROXIDE	en
dc.subject	MALEIMIDE DERIVATIVE	en
dc.subject	ANTIOXIDANT ACTIVITY	en
dc.subject	CONTROLLED STUDY	en
dc.subject	DRUG MECHANISM	en
dc.subject	DRUG SYNTHESIS	en
dc.subject	IN VITRO STUDY	en
dc.subject	MICROWAVE ASSISTED SYNTHESIS	en
dc.subject	STRUCTURE ACTIVITY RELATION	en
dc.subject	SUBSTITUTION REACTION	en
dc.subject	SYNTHESIS	en
dc.title	Microwave-Assisted Synthesis of N-Substituted Maleimide Derivatives as Exogenous Antioxidant Agents	en
dc.type	Article	en
dc.type	info:eu-repo/semantics/article	en
dc.type	info:eu-repo/semantics/publishedVersion	en
dc.identifier.doi	10.1002/jhet.3421	-
dc.identifier.scopus	85057838110	-
local.contributor.employee	Rammohan, A., Department of Physical Sciences, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India, Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employee	Mallikarjuna Reddy, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation, Department of Chemistry, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil
local.contributor.employee	Raul Garcia, J., Department of Chemistry, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil
local.contributor.employee	Zyryanov, G.V., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation, Ural Division of the Russian Academy of Sciences, I. Ya. Postovskiy Institute of Organic Synthesis, 22 S. Kovalevskoy Street, Yekaterinburg, Russian Federation
local.contributor.employee	Sravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employee	Bakthavatchala Reddy, N., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employee	Yuvaraja, G., School of Environmental Science and Engineering, Guangdong Provincial Key Laboratory for Radionuclides Pollution Control and Resources, Guangzhou University, Guangzhou, 510006, China
local.description.firstpage	470	-
local.description.lastpage	476	-
local.issue	2	-
local.volume	56	-
local.contributor.department	Department of Physical Sciences, Sri Padmavati Mahila Visvavidyalayam, Tirupati, India
local.contributor.department	Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.department	Department of Chemistry, State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil
local.contributor.department	Ural Division of the Russian Academy of Sciences, I. Ya. Postovskiy Institute of Organic Synthesis, 22 S. Kovalevskoy Street, Yekaterinburg, Russian Federation
local.contributor.department	School of Environmental Science and Engineering, Guangdong Provincial Key Laboratory for Radionuclides Pollution Control and Resources, Guangzhou University, Guangzhou, 510006, China
local.identifier.pure	9055456	-
local.identifier.pure	4b20a18f-9795-4954-a2ee-08d58d18d5f3	uuid
local.identifier.eid	2-s2.0-85057838110	-
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