Hydrodifluoromethylation of alkenes with difluoroacetic acid
A facile method for the regioselective hydrodifluoromethylation of alkenes is reported using difluoroacetic acid and phenyliodine(III) diacetate in tetrahydrofuran under visible‐light activation. This metal‐free approach stands out as it uses inexpensive reagents, does not require a photocatalyst, a...
| Main Authors: | , , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
Wiley
2019
|
| _version_ | 1797091165298753536 |
|---|---|
| author | Meyer, C Hell, S Misale, A Trabanco, A Gouverneur, V |
| author_facet | Meyer, C Hell, S Misale, A Trabanco, A Gouverneur, V |
| author_sort | Meyer, C |
| collection | OXFORD |
| description | A facile method for the regioselective hydrodifluoromethylation of alkenes is reported using difluoroacetic acid and phenyliodine(III) diacetate in tetrahydrofuran under visible‐light activation. This metal‐free approach stands out as it uses inexpensive reagents, does not require a photocatalyst, and displays broad functional group tolerance. The procedure is also operationally simple and scalable, and provides access in one step to high‐value building blocks for application in medicinal chemistry. |
| first_indexed | 2024-03-07T03:29:07Z |
| format | Journal article |
| id | oxford-uuid:ba1421fa-3d9b-4c2f-923a-aad806535c32 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:29:07Z |
| publishDate | 2019 |
| publisher | Wiley |
| record_format | dspace |
| spelling | oxford-uuid:ba1421fa-3d9b-4c2f-923a-aad806535c322022-03-27T05:07:33ZHydrodifluoromethylation of alkenes with difluoroacetic acidJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ba1421fa-3d9b-4c2f-923a-aad806535c32EnglishSymplectic Elements at OxfordWiley2019Meyer, CHell, SMisale, ATrabanco, AGouverneur, VA facile method for the regioselective hydrodifluoromethylation of alkenes is reported using difluoroacetic acid and phenyliodine(III) diacetate in tetrahydrofuran under visible‐light activation. This metal‐free approach stands out as it uses inexpensive reagents, does not require a photocatalyst, and displays broad functional group tolerance. The procedure is also operationally simple and scalable, and provides access in one step to high‐value building blocks for application in medicinal chemistry. |
| spellingShingle | Meyer, C Hell, S Misale, A Trabanco, A Gouverneur, V Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title | Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title_full | Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title_fullStr | Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title_full_unstemmed | Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title_short | Hydrodifluoromethylation of alkenes with difluoroacetic acid |
| title_sort | hydrodifluoromethylation of alkenes with difluoroacetic acid |
| work_keys_str_mv | AT meyerc hydrodifluoromethylationofalkeneswithdifluoroaceticacid AT hells hydrodifluoromethylationofalkeneswithdifluoroaceticacid AT misalea hydrodifluoromethylationofalkeneswithdifluoroaceticacid AT trabancoa hydrodifluoromethylationofalkeneswithdifluoroaceticacid AT gouverneurv hydrodifluoromethylationofalkeneswithdifluoroaceticacid |