Azaanthracenes via Inverse Electron-Demand Diels–Alder Reaction

dc.contributor.authorKopchuk, Dmitry S.
dc.contributor.authorChepchugov, N. V.
dc.contributor.authorTaniya, Olga S.
dc.contributor.authorKhasanov, A.F.
dc.contributor.authorGiri,Kousik
dc.contributor.authorKovalev, Igor S.
dc.contributor.authorSantra, S.
dc.contributor.authorZyryanov, Grigory V.
dc.contributor.authorMajee, A.
dc.contributor.authorRusinov, V.L.
dc.contributor.authorChupakhin, O.N.
dc.date.accessioned2018-01-31T07:31:02Z
dc.date.accessioned2024-08-13T11:13:30Z
dc.date.available2018-01-31T07:31:02Z
dc.date.available2024-08-13T11:13:30Z
dc.date.issued2016
dc.description.abstractSignificance: Azaanthracenes are important fluo- Comment: The benzyne derivative is generated in rophores that are used in a number of applications such as metal or pH sensors. In this report the authors describe a new synthesis of this type of structure via an inverse electron-demand aza- Diels–Alder reaction between a benzyne derivative and an electron-deficient triazine. situ from the diazotization of 2-amino-3-naphthoic acid. It was found that the cyano activating group at the 5-position of the triazine is crucial for the reaction to take place because it offers a smaller energy difference between the cycloaddition HOMO and LUMO.en_US
dc.identifier.citationKopchuk, D.S., Chepchugov, N.V., Taniya, O.S. and et. al. Azaanthracenes via Inverse Electron-Demand Diels–Alder Reaction(2016) Tetrahedron Lett. 2016 , 57, 5639–5643.en_US
dc.identifier.issn0040-4039
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/552
dc.language.isoenen_US
dc.publisherTHIEME STUTTGARTen_US
dc.subjectaza-Diels–Alder reactionen_US
dc.subjecttriazinesen_US
dc.subjectfluorophoresen_US
dc.titleAzaanthracenes via Inverse Electron-Demand Diels–Alder Reactionen_US
dc.typeArticleen_US

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