Abstract
A cobalt-catalyzed acylation reaction of various primary, secondary and tertiary alkyl, benzyl and (hetero)aryl S-pyridyl thioesters with (hetero)arylzinc pivalates is reported. The thioesters were prepared directly from the corresponding carboxylic acids under mild conditions, thus tolerating sensitive functional groups. Acylations of alpha-chiral S-pyridyl esters proceeded with very high stereoretention leading to optically enriched alpha-chiral ketones.
| Item Type: | Journal article |
|---|---|
| Faculties: | Chemistry and Pharmacy > Department of Chemistry |
| Subjects: | 500 Science > 540 Chemistry |
| ISSN: | 2041-6520 |
| Language: | English |
| Item ID: | 83312 |
| Date Deposited: | 15. Dec 2021 15:07 |
| Last Modified: | 15. Dec 2021 15:07 |
