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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol101720e
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dc.titleFused bispentacenequinone and its unexpected Michael addition
dc.contributor.authorZhang, X.
dc.contributor.authorLi, J.
dc.contributor.authorQu, H.
dc.contributor.authorChi, C.
dc.contributor.authorWu, J.
dc.date.accessioned2014-06-23T05:40:16Z
dc.date.available2014-06-23T05:40:16Z
dc.date.issued2010-09-03
dc.identifier.citationZhang, X., Li, J., Qu, H., Chi, C., Wu, J. (2010-09-03). Fused bispentacenequinone and its unexpected Michael addition. Organic Letters 12 (17) : 3946-3949. ScholarBank@NUS Repository. https://doi.org/10.1021/ol101720e
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76235
dc.description.abstractFused bispentacenequinone 2 was synthesized by photocyclization of bispentacenequinone 1. Unusual regioselective Michael addition was observed for 2 when excess aryl Grignard reagent was used. Subsequent acidification and oxidation in air gave diaryl-substituted bispentacenequinone 3. Tetra-aryl-substituted fused bispentacenequinone 4 was obtained from 3 after the second Michael addition followed by oxidation in air. © 2010 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol101720e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol101720e
dc.description.sourcetitleOrganic Letters
dc.description.volume12
dc.description.issue17
dc.description.page3946-3949
dc.identifier.isiut000281180700056
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