Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3
A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Beilstein-Institut
2013-12-01
|
| Series: | Beilstein Journal of Organic Chemistry |
| Subjects: | |
| Online Access: | https://doi.org/10.3762/bjoc.9.322 |
| _version_ | 1818414511277735936 |
|---|---|
| author | Xueliang Jiang Feng-Ling Qing |
| author_facet | Xueliang Jiang Feng-Ling Qing |
| author_sort | Xueliang Jiang |
| collection | DOAJ |
| description | A Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds. |
| first_indexed | 2024-12-14T11:20:15Z |
| format | Article |
| id | doaj.art-8adcfce679754aee91d2a79f52f7cdff |
| institution | Directory Open Access Journal |
| issn | 1860-5397 |
| language | English |
| last_indexed | 2024-12-14T11:20:15Z |
| publishDate | 2013-12-01 |
| publisher | Beilstein-Institut |
| record_format | Article |
| series | Beilstein Journal of Organic Chemistry |
| spelling | doaj.art-8adcfce679754aee91d2a79f52f7cdff2022-12-21T23:03:47ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972013-12-01912862286510.3762/bjoc.9.3221860-5397-9-322Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3Xueliang Jiang0Feng-Ling Qing1Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, ChinaKey Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, ChinaA Cu-mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 was developed for the first time. This method offers a convenient and economical approach to various trifluoroethyl-containing compounds.https://doi.org/10.3762/bjoc.9.322coppermethanesulfonatesorgano-fluorinetrifluoromethylation |
| spellingShingle | Xueliang Jiang Feng-Ling Qing Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 Beilstein Journal of Organic Chemistry copper methanesulfonates organo-fluorine trifluoromethylation |
| title | Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 |
| title_full | Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 |
| title_fullStr | Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 |
| title_full_unstemmed | Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 |
| title_short | Cu-Mediated trifluoromethylation of benzyl, allyl and propargyl methanesulfonates with TMSCF3 |
| title_sort | cu mediated trifluoromethylation of benzyl allyl and propargyl methanesulfonates with tmscf3 |
| topic | copper methanesulfonates organo-fluorine trifluoromethylation |
| url | https://doi.org/10.3762/bjoc.9.322 |
| work_keys_str_mv | AT xueliangjiang cumediatedtrifluoromethylationofbenzylallylandpropargylmethanesulfonateswithtmscf3 AT fenglingqing cumediatedtrifluoromethylationofbenzylallylandpropargylmethanesulfonateswithtmscf3 |