Iridium‐Catalyzed <i>α</i>‐C–H Alkenylation of Alkylamines with Alkynes Followed by Alkene Isomerization Into Enamines

The iridium‐catalyzed intermolecular α ‐C–H alkenylation of N ‐methyl‐2‐aminopyridine derivatives proceeds via alkene isomerization to give the corresponding enamines. The reaction is efficiently catalyzed by a cationic iridium catalyst under mild reaction conditions. The same catalytic system can also be applied to the intramolecular C–H addition to alkynes to give cyclic ketones after hydrolysis of the corresponding enamines.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-08-15
DOI
https://doi.org/10.1002/adsc.70055
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Iridium‐Catalyzed α‐C–H Alkenylation of Alkylamines with Alkynes Followed by Alkene Isomerization Into Enamines

Takahiro Nishimura, Yuki Takahashi, Kentaro Yamakawa
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

Iridium‐Catalyzed α‐C–H Alkenylation of Alkylamines with Alkynes Followed by Alkene Isomerization Into Enamines

Takahiro Nishimura, Yuki Takahashi, Kentaro Yamakawa
article en

Abstract

The iridium‐catalyzed intermolecular α ‐C–H alkenylation of N ‐methyl‐2‐aminopyridine derivatives proceeds via alkene isomerization to give the corresponding enamines. The reaction is efficiently catalyzed by a cationic iridium catalyst under mild reaction conditions. The same catalytic system can also be applied to the intramolecular C–H addition to alkynes to give cyclic ketones after hydrolysis of the corresponding enamines.

Advanced Synthesis & Catalysis
Tokyo Metropolitan University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 84%
Catalytic C–H Functionalization Methods
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