Abstract
We describe a novel triethylamine catalyzed S → O acetyl migration reaction for yielding thiol compounds under mild conditions through the formation of a transitional 5-membered ring. A series of epoxy compounds have been transformed into their thiol counterparts which could be used for construction of topological and functional sulfur-containing polymers. The one-pot two-step processes including the S → O acetyl migration and the following thiol-click reactions avoided separation of thiol intermediates. Applying these processes on a new-type latent polythiols overcomes crosslinking problem usually met in preparation of multithiol compounds due to the formation of disulfide bonds. This journal is
| Original language | English |
|---|---|
| Pages (from-to) | 5674-5679 |
| Number of pages | 6 |
| Journal | RSC Advances |
| Volume | 5 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 1 Jan 2015 |