Abstract
A novel reagent, which introduces two sulfur atoms in one step, was designed and used for the construction of diverse disulfanes by copper-catalyzed oxidative cross-coupling under mild reaction conditions. By applying this stable and readily prepared reagent, late-stage modification of pharmaceuticals and natural products can be achieved straightforward. The scaled-up experiments further indicated the practicality of this protocol. The pH value of the system plays a key role in achieving highly selective cleavage of the C−S bond instead of a S−S bond in the transformation.
| Original language | English |
|---|---|
| Pages (from-to) | 14121-14125 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 55 |
| Issue number | 45 |
| DOIs | |
| State | Published - 2 Nov 2016 |
Keywords
- copper
- cross-coupling
- disulfuration
- sulfur
- synthetic methods