Pd‐Catalyzed Regioselective Isomerization‐Hydroformylation of Internal Olefins with <scp> HCO <sub>2</sub> H </scp> and <i>N</i> ‐Formylsaccharin
Comprehensive Summary This work describes an effective Pd‐catalyzed isomerization‐hydroformylation of internal olefins with HCO 2 H and N ‐formylsaccharin, providing a wide variety of linear aldehydes in up to 72% yield with up to 18 : 1 l/b ratio. The olefin substrate can bear various functional groups. Conjugated olefins can also be efficiently isomerized and hydroformylated. The reaction is easy to operate and requires no handling of CO and H 2 . To the best of our knowledge, the current process represents the first example for Pd‐catalyzed efficient isomerization‐hydroformylation process of internal olefins to predominately give linear aldehydes.
Authors
- Wenlong Ren (ORCID: https://orcid.org/0000-0002-2028-4667)
- Yian Shi (ORCID: https://orcid.org/0000-0001-9016-2078)
- Jinzi Huang
- Yuan Shi (ORCID: https://orcid.org/0009-0009-8491-3838)
- Jintao Ou
Institutions
- Changzhou University (CN)
Publication Details
- Journal
- Chinese Journal of Chemistry
- Published
- 2025-09-16
- DOI
- https://doi.org/10.1002/cjoc.70248
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00