http://10.10.120.238:8080/xmlui/handle/123456789/533
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hussain Y. | en_US |
dc.contributor.author | Sharma D. | en_US |
dc.contributor.author | Tamanna N. | en_US |
dc.contributor.author | Chauhan P. | en_US |
dc.date.accessioned | 2023-11-30T08:40:59Z | - |
dc.date.available | 2023-11-30T08:40:59Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.other | EID(2-s2.0-85152211098) | - |
dc.identifier.uri | https://dx.doi.org/10.1021/acs.orglett.3c00685 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/533 | - |
dc.description.abstract | An 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.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.source | Organic Letters | en_US |
dc.title | Relay Organophotoredox/N-Heterocyclic Carbene Catalysis-Enabled Asymmetric Synthesis of Dibenzoxazepine-Fused Pyrrolidinones | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Journal Article |
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