Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Uno, Misae | en_US |
dc.contributor.author | Sumino, Shuhei | en_US |
dc.contributor.author | Fukuyama, Takahide | en_US |
dc.contributor.author | Matsuura, Makoto | en_US |
dc.contributor.author | Kuroki, Yoshichika | en_US |
dc.contributor.author | Kishikawa, Yosuke | en_US |
dc.contributor.author | Ryu, Ilhyong | en_US |
dc.date.accessioned | 2019-09-02T07:46:16Z | - |
dc.date.available | 2019-09-02T07:46:16Z | - |
dc.date.issued | 2019-07-19 | en_US |
dc.identifier.issn | 0022-3263 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/acs.joc.9b00901 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/152661 | - |
dc.description.abstract | Photoredox-catalyzed allylation of alpha-gem-difluorinated organohalides with allyl sulfones proceeded smoothly under visible light irradiation to give 4,4-difluoroalkenes in good yields. In the presence of catalytic Ru(bpy)(3)Cl-2, Hantzsch ester, and diisopropylethylamine, the reaction was complete within 2 h. Using the same methodology, three-component cascade reactions to give 6,6-difluoroalkenes were carried out successfully. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Synthesis of 4,4-Difluoroalkenes by Coupling of alpha-Substituted alpha,alpha-Difluoromethyl Halides with Allyl Sulfones under Photoredox Catalyzed Conditions | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/acs.joc.9b00901 | en_US |
dc.identifier.journal | JOURNAL OF ORGANIC CHEMISTRY | en_US |
dc.citation.volume | 84 | en_US |
dc.citation.issue | 14 | en_US |
dc.citation.spage | 9330 | en_US |
dc.citation.epage | 9338 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000476957000047 | en_US |
dc.citation.woscount | 0 | en_US |
Appears in Collections: | Articles |