Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 13, Issue 3, Pages 677-681Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ob02250e
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An unprecedented C-S formation method via direct oxidative C(sp(3))-H bond functionalization and C-O cleavage of benzylic ethers was developed. Various thioesters including thioester structure containing drug intermediates could be achieved by this convenient, metal and base free method in satisfactory yields.
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