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.

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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
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article

Pd‐Catalyzed Regioselective Isomerization‐Hydroformylation of Internal Olefins with HCO 2 H and N ‐Formylsaccharin

Wenlong Ren, Yian Shi, Jinzi Huang, Yuan Shi et al.
Chinese Journal of Chemistry
Asymmetric Hydrogenation and Catalysis
article

Pd‐Catalyzed Regioselective Isomerization‐Hydroformylation of Internal Olefins with HCO 2 H and N ‐Formylsaccharin

Wenlong Ren, Yian Shi, Jinzi Huang, Yuan Shi, Jintao Ou
article en

Abstract

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.

Chinese Journal of ChemistryVol. 43(23)
Changzhou University (CN)
Openalex Percentile: Top 79%
Asymmetric Hydrogenation and Catalysis
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