Abstract
The direct functionalization of inert sp3CH bonds is limited to a few bond types. Although the activation of sp3CH bonds can be accomplished under mild conditions using palladium catalysts, the subsequent functionalization is not trivial due to the high energy required to convert palladium(II) to palladium(IV). We have systematically studied the palladium oxidation using computation-guided experiments for reactions involving strong chelation control. We find that a mild external ligand could significantly accelerate the oxidation of palladium(II) to palladium(IV) for strong bidentate directing groups. The acceleration is believed to be a result of ligand stabilization of both the palladium(II) and palladium(IV) intermediates. (Figure presented.) .
| Original language | English |
|---|---|
| Pages (from-to) | 1946-1957 |
| Number of pages | 12 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 358 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 16 Jun 2016 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
- CH activation
- directing group
- fluorination
- oxidation
- palladium
Fingerprint
Dive into the research topics of 'Ligand-Assisted Palladium(II)/(IV) Oxidation for sp3CH Fluorination'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver