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https://hdl.handle.net/10356/137777
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DC Field | Value | Language |
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dc.contributor.author | Wang, Hongling | en_US |
dc.contributor.author | Wang, Yuhuang | en_US |
dc.contributor.author | Chen, Xingkuan | en_US |
dc.contributor.author | Mou, Chengli | en_US |
dc.contributor.author | Yu, Shuyan | en_US |
dc.contributor.author | Chai, Huifang | en_US |
dc.contributor.author | Jin, Zhichao | en_US |
dc.contributor.author | Chi, Robin Yonggui | en_US |
dc.date.accessioned | 2020-04-14T06:45:30Z | - |
dc.date.available | 2020-04-14T06:45:30Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Wang, H., Wang, Y., Chen, X., Mou, C., Yu, S., Chai, H., ... , Chi, R. Y. (2019). Chiral nitroarenes as enantioselective single-electron-transfer oxidants for carbene-catalyzed radical reactions. Organic Letters, 21(18), 7440-7444. doi:10.1021/acs.orglett.9b02736 | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | https://hdl.handle.net/10356/137777 | - |
dc.description.abstract | A new class of chiral oxidants is developed. These readily accessible oxidants contain a nitro group for oxidation and a chiral sulfonamide moiety for stereoselectivity control. The chiral information from the oxidants can effectively transfer to the substrates in carbene-catalyzed β-hydroxylation of enals via single-electron-transfer radical processes. We expect these oxidants to find unique applications in other asymmetric oxidations and oxygen-atom-transferring reactions. | en_US |
dc.description.sponsorship | NRF (Natl Research Foundation, S’pore) | en_US |
dc.description.sponsorship | ASTAR (Agency for Sci., Tech. and Research, S’pore) | en_US |
dc.description.sponsorship | MOE (Min. of Education, S’pore) | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Organic Letters | en_US |
dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.9b02736 | en_US |
dc.subject | Science::Chemistry::Organic chemistry | en_US |
dc.title | Chiral nitroarenes as enantioselective single-electron-transfer oxidants for carbene-catalyzed radical reactions | en_US |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en_US |
dc.identifier.doi | 10.1021/acs.orglett.9b02736 | - |
dc.description.version | Accepted version | en_US |
dc.identifier.pmid | 31478384 | - |
dc.identifier.scopus | 2-s2.0-85072546160 | - |
dc.identifier.issue | 18 | en_US |
dc.identifier.volume | 21 | en_US |
dc.identifier.spage | 7440 | en_US |
dc.identifier.epage | 7444 | en_US |
dc.subject.keywords | Enantioselective | en_US |
dc.subject.keywords | Chirality | en_US |
item.fulltext | With Fulltext | - |
item.grantfulltext | open | - |
Appears in Collections: | SPMS Journal Articles |
Files in This Item:
File | Description | Size | Format | |
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Chiral Nitroarenes as Enantioselective Single-Electron-Transfer Oxidants for Carbene-Catalyzed Radical Reactions.pdf | 1.02 MB | Adobe PDF | View/Open |
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