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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/533
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dc.contributor.authorHussain Y.en_US
dc.contributor.authorSharma D.en_US
dc.contributor.authorTamanna N.en_US
dc.contributor.authorChauhan P.en_US
dc.date.accessioned2023-11-30T08:40:59Z-
dc.date.available2023-11-30T08:40:59Z-
dc.date.issued2023-
dc.identifier.issn1523-7060-
dc.identifier.otherEID(2-s2.0-85152211098)-
dc.identifier.urihttps://dx.doi.org/10.1021/acs.orglett.3c00685-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/533-
dc.description.abstractAn unprecedented highly stereoselective synthesis of pyrrolo[1,2-d][1,4]oxazepin-3(2H)-ones has been accomplished via photoredox/N-heterocyclic carbene (NHC) relay catalysis. A wide range of substituted dibenzoxazepines and aryl/hetereoaryl enals were well accommodated under the organic photoredox catalysis-promoted amine oxidation to generate the imines, followed by a NHC-catalyzed [3 + 2] annulation reaction to achieve excellent diastereo- and enantioselectivities of the dibenzoxazepine-fused pyrrolidinones. © 2023 American Chemical Society.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceOrganic Lettersen_US
dc.titleRelay Organophotoredox/N-Heterocyclic Carbene Catalysis-Enabled Asymmetric Synthesis of Dibenzoxazepine-Fused Pyrrolidinonesen_US
dc.typeJournal Articleen_US
Appears in Collections:Journal Article

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