Tethered aminohydroxylation (TA) reaction of amides.
The first examples of amide-tethered aminohydroxylation reactions, catalyzed by osmium, showing that the use of N-O-based reoxidants are essential for success, are reported. The system that is described is compatible with a variety of different alkene substitution patterns and ring sizes and works w...
| Main Authors: | , , |
|---|---|
| 格式: | Journal article |
| 语言: | English |
| 出版: |
2009
|
| _version_ | 1826259628296503296 |
|---|---|
| author | Donohoe, T Callens, C Thompson, A |
| author_facet | Donohoe, T Callens, C Thompson, A |
| author_sort | Donohoe, T |
| collection | OXFORD |
| description | The first examples of amide-tethered aminohydroxylation reactions, catalyzed by osmium, showing that the use of N-O-based reoxidants are essential for success, are reported. The system that is described is compatible with a variety of different alkene substitution patterns and ring sizes and works with low loadings in both cyclic and acyclic systems. The levels of diastereoselectivity that were observed for substituents at both the allylic and homallylic position bode well for the use of stereoselective TA reactions in organic synthesis. |
| first_indexed | 2024-03-06T18:52:52Z |
| format | Journal article |
| id | oxford-uuid:10d8dc5c-ed76-4c86-94d8-c7dae579a6a5 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T18:52:52Z |
| publishDate | 2009 |
| record_format | dspace |
| spelling | oxford-uuid:10d8dc5c-ed76-4c86-94d8-c7dae579a6a52022-03-26T09:58:43ZTethered aminohydroxylation (TA) reaction of amides.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:10d8dc5c-ed76-4c86-94d8-c7dae579a6a5EnglishSymplectic Elements at Oxford2009Donohoe, TCallens, CThompson, AThe first examples of amide-tethered aminohydroxylation reactions, catalyzed by osmium, showing that the use of N-O-based reoxidants are essential for success, are reported. The system that is described is compatible with a variety of different alkene substitution patterns and ring sizes and works with low loadings in both cyclic and acyclic systems. The levels of diastereoselectivity that were observed for substituents at both the allylic and homallylic position bode well for the use of stereoselective TA reactions in organic synthesis. |
| spellingShingle | Donohoe, T Callens, C Thompson, A Tethered aminohydroxylation (TA) reaction of amides. |
| title | Tethered aminohydroxylation (TA) reaction of amides. |
| title_full | Tethered aminohydroxylation (TA) reaction of amides. |
| title_fullStr | Tethered aminohydroxylation (TA) reaction of amides. |
| title_full_unstemmed | Tethered aminohydroxylation (TA) reaction of amides. |
| title_short | Tethered aminohydroxylation (TA) reaction of amides. |
| title_sort | tethered aminohydroxylation ta reaction of amides |
| work_keys_str_mv | AT donohoet tetheredaminohydroxylationtareactionofamides AT callensc tetheredaminohydroxylationtareactionofamides AT thompsona tetheredaminohydroxylationtareactionofamides |