1. Электронный научный архив УрФУ
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  3. Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC
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dc.contributor.authorRammohan, A.en
dc.contributor.authorKhasanov, A. F.en
dc.contributor.authorKopchuk, D. S.en
dc.contributor.authorGunasekar, D.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorChupakhin, O. N.en
dc.date.accessioned2022-10-19T05:19:39Z-
dc.date.available2022-10-19T05:19:39Z-
dc.date.issued2022-
dc.identifier.citationAssessment on facile Diels–Alder approach of α-pyrone and terpenoquinone for the expedient synthesis of various natural scaffolds / A. Rammohan, A. F. Khasanov, D. S. Kopchuk et al. // Natural Products and Bioprospecting. — 2022. — Vol. 12. — Iss. 1. — 12.en
dc.identifier.issn21922195-
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85127512237&doi=10.1007%2fs13659-022-00333-4&partnerID=40&md5=6b7eead82d72568c35d3c67819999176link
dc.identifier.urihttp://elar.urfu.ru/handle/10995/117814-
dc.description.abstractThe development of highly facile synthetic procedures for the expedient synthesis of complex natural molecules is always in demand. As this aspect, the Diels–Alder reaction (DAR) has a versatile approach to the synthesis of complex natural compounds and highly regio-/stereoselcetive heterocyclic scaffolds. Additionally, α-pyrone and terpenoquinone are two versatile key intermediates that are prevalent in various bioactive natural compounds for instance, (±)-crinine, (±)-joubertinamine, (±)-pancratistatin, (−)-cyclozonarone, and 8-ephipuupehedione, etc. Hence, the current review summarizes the Diels–Alder reaction application of α-pyrone and terpenoquinone to the constructive synthesis of various natural products over the past two decades (2001–2021). Equally, it serves as a stencil for the invention and development of new synthetic strategies for high-complex molecular structured natural and heterocyclic molecules. Graphical Abstract: [Figure not available: see fulltext.] © 2022, The Author(s).en
dc.description.sponsorshipRussian Science Foundation, RSF; Council on grants of the President of the Russian Federation: 21-13-00304, HШ-2700.2020.3en
dc.description.sponsorshipThis work was financially supported by the Grants Council of the President of the Russian Federation (# HШ-2700.2020.3) and Russian Scientific Foundation (Grant # 21-13-00304).en
dc.description.sponsorshipCouncil on grants of the President of the Russian Federation, HШ-2700.2020.3, Zyryanov Grigory V., Российский Фонд Фундаментальных Исследований (РФФИ), Grant # 21-13-00304, Zyryanov Grigory V.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherSpringeren
dc.relationinfo:eu-repo/grantAgreement/RSF//21-13-00304en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceNatural Products and Bioprospectingen
dc.subjectDIELS–ALDER REACTION (DAR)en
dc.subjectMARINE NATURAL COMPOUNDSen
dc.subjectTERPENOQUINONEen
dc.subjectTOTAL SYNTHESISen
dc.subjectΑ-PYRONEen
dc.titleAssessment on facile Diels–Alder approach of α-pyrone and terpenoquinone for the expedient synthesis of various natural scaffoldsen
dc.typeReviewen
dc.typeinfo:eu-repo/semantics/reviewen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1007/s13659-022-00333-4-
dc.identifier.scopus85127512237-
local.contributor.employeeRammohan, A., Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation, Natural Products Division, Department of Chemistry, Sri Venkateswara University, Tirupati, 517502, Indiaen
local.contributor.employeeKhasanov, A.F., Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation, Ural Division of the Russian Academy of Sciences, I. Ya. Postovsky Institute of Organic Synthesis, 22 S. Kovalevskoy St., Ekaterinburg, 620219, Russian Federationen
local.contributor.employeeKopchuk, D.S., Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation, Ural Division of the Russian Academy of Sciences, I. Ya. Postovsky Institute of Organic Synthesis, 22 S. Kovalevskoy St., Ekaterinburg, 620219, Russian Federationen
local.contributor.employeeGunasekar, D., Natural Products Division, Department of Chemistry, Sri Venkateswara University, Tirupati, 517502, Indiaen
local.contributor.employeeZyryanov, G.V., Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation, Ural Division of the Russian Academy of Sciences, I. Ya. Postovsky Institute of Organic Synthesis, 22 S. Kovalevskoy St., Ekaterinburg, 620219, Russian Federationen
local.contributor.employeeChupakhin, O.N., Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation, Ural Division of the Russian Academy of Sciences, I. Ya. Postovsky Institute of Organic Synthesis, 22 S. Kovalevskoy St., Ekaterinburg, 620219, Russian Federationen
local.issue1-
local.volume12-
dc.identifier.wos000776718400002-
local.contributor.departmentUral Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federationen
local.contributor.departmentNatural Products Division, Department of Chemistry, Sri Venkateswara University, Tirupati, 517502, Indiaen
local.contributor.departmentUral Division of the Russian Academy of Sciences, I. Ya. Postovsky Institute of Organic Synthesis, 22 S. Kovalevskoy St., Ekaterinburg, 620219, Russian Federationen
local.identifier.pure29924988-
local.description.order12-
local.identifier.eid2-s2.0-85127512237-
local.fund.rsf21-13-00304-
local.identifier.wosWOS:000776718400002-
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