Cobalt‐Catalyzed C(sp <sup>3</sup> )H Carbonylation Enabled by Mo(CO) <sub>6</sub>

The carbonylation of unactivated C(sp 3 )H bonds represents an attractive strategy for the synthesis of valuable carbonyl‐containing compounds. Herein, we report a cobalt‐catalyzed 8‐aminoquinoline‐directed carbonylative C(sp 3 )H cyclization of aliphatic amides using Mo(CO) 6 as a practical solid CO surrogate. This atom‐economical protocol provides straightforward access to substituted succinimides in good‐to‐excellent yields, employing low cobalt catalyst loadings (5 mol%). The reaction proceeds under operationally simple conditions and avoids the direct handling of gaseous carbon monoxide. To the best of our knowledge, this study represents the first example of a cobalt‐catalyzed C(sp 3 )H carbonylative transformation using Mo(CO) 6 as the carbon monoxide source.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-08-17
DOI
https://doi.org/10.1002/ejoc.70744
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Cobalt‐Catalyzed C(sp 3 )H Carbonylation Enabled by Mo(CO) 6

Javier Adrio, Nuria Rodríguez, Inés Alonso, Juan C. Carretero et al.
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

Cobalt‐Catalyzed C(sp 3 )H Carbonylation Enabled by Mo(CO) 6

Javier Adrio, Nuria Rodríguez, Inés Alonso, Juan C. Carretero, Emma Duro
article en

Abstract

The carbonylation of unactivated C(sp 3 )H bonds represents an attractive strategy for the synthesis of valuable carbonyl‐containing compounds. Herein, we report a cobalt‐catalyzed 8‐aminoquinoline‐directed carbonylative C(sp 3 )H cyclization of aliphatic amides using Mo(CO) 6 as a practical solid CO surrogate. This atom‐economical protocol provides straightforward access to substituted succinimides in good‐to‐excellent yields, employing low cobalt catalyst loadings (5 mol%). The reaction proceeds under operationally simple conditions and avoids the direct handling of gaseous carbon monoxide. To the best of our knowledge, this study represents the first example of a cobalt‐catalyzed C(sp 3 )H carbonylative transformation using Mo(CO) 6 as the carbon monoxide source.

European Journal of Organic Chemistry
Institute of Advanced Chemistry of Catalonia (ES), Universidad Autónoma de Madrid (ES)
Ministerio de Ciencia, Innovación y Universidades
Openalex Percentile: Top 18%
Catalytic C–H Functionalization Methods
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