Difluoromethanesulfonyl hypervalent iodoniumylides for electrophilic difluoromethylthiolation reactions under copper catalysis
dc.contributor.author | Arimori, Sadayuki | en_US |
dc.contributor.author | Matsubara, Okiya | en_US |
dc.contributor.author | Takada, Masahiro | en_US |
dc.date.accessioned | 2016-07-04T03:49:04Z | |
dc.date.available | 2016-07-04T03:49:04Z | |
dc.date.issued | 2016 | en_US |
dc.identifier.other | HPU4160388 | en_US |
dc.identifier.uri | https://lib.hpu.edu.vn/handle/123456789/21905 | |
dc.description.abstract | Difluoromethanesulfonyl hypervalent iodonium ylides 2 were developed as electrophilic difluoromethylthiolation reagents for a wide range of nucleophiles. Enamines, indoles, β-keto esters, silyl enol ethers and pyrroles were effectively reacted with2affording desired difluoromethylthio (SCF2H)-substituted compounds in good to high yields under copper catalysis. | en_US |
dc.format.extent | 9 p. | en_US |
dc.format.mimetype | application/pdf | |
dc.language.iso | en | en_US |
dc.subject | Organic chemistry | en_US |
dc.subject | Synthetic | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Organometallic chemistry | en_US |
dc.subject | Difluoromethylthiolation | en_US |
dc.subject | Hypervalent | en_US |
dc.subject | Iodoniumylide | en_US |
dc.subject | Carbene | en_US |
dc.subject | Sulfur | en_US |
dc.subject | Fluorine | en_US |
dc.title | Difluoromethanesulfonyl hypervalent iodoniumylides for electrophilic difluoromethylthiolation reactions under copper catalysis | en_US |
dc.type | Article | en_US |
dc.size | 764KB | en_US |
dc.department | Education | en_US |
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