This decommissioned ERA site remains active temporarily to support our final migration steps to https://ualberta.scholaris.ca, ERA's new home. All new collections and items, including Spring 2025 theses, are at that site. For assistance, please contact erahelp@ualberta.ca.
Communities and Collections
Usage
- 115 views
- 348 downloads
Formation of Enol Ethers by Radical Decarboxylation of α-Alkoxy β-Phenylthio Acids
-
- Author(s) / Creator(s)
-
Enol ethers are formed by radical decarboxylation of α-alkoxy β-phenylthio acids via the corresponding Barton esters. The phenylthio acids were usually made by the known regioselective reaction of α,β-epoxy acids with PhSH in the presence of InCl3, followed by O-alkylation of the resulting alcohol. In one case, thiol addition to an α,β-unsaturated ethoxymethyl ester was used.
-
- Date created
- 2019-08-29
-
- Subjects / Keywords
-
- Type of Item
- Article (Draft / Submitted)
-
- License
- © American Chemical Society, 2019. This is an open access article which is free to download and share.