Carboxylative cyclization of propargylamines with carbamate salts as a non-gaseous CO2 source via dual-activation by Ag salts

Abstract 2-Oxazolidinones were synthesized from propargylamines using carbamate salts as the CO2 source. Ag catalysts act as activators for both alkynes and carbamate salts. This system also functions with aliphatic amines containing two or more nitrogen atoms by preparing carbamate salts in situ even under ambient conditions.

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Publication Details

Journal
Chemistry Letters
Published
2025-01-27
DOI
https://doi.org/10.1093/chemle/upaf007
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70
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article

Carboxylative cyclization of propargylamines with carbamate salts as a non-gaseous CO2 source via dual-activation by Ag salts

Asami Yoshii, Akira Fujii, Ryuki Baba, Yasuhiro Nishiyama et al.
1 citations
Chemistry Letters
Carbon dioxide utilization in catalysis
0.70
article

Carboxylative cyclization of propargylamines with carbamate salts as a non-gaseous CO2 source via dual-activation by Ag salts

Asami Yoshii, Akira Fujii, Ryuki Baba, Yasuhiro Nishiyama, Hajime Mori
article en
1 citations

Abstract

Abstract 2-Oxazolidinones were synthesized from propargylamines using carbamate salts as the CO2 source. Ag catalysts act as activators for both alkynes and carbamate salts. This system also functions with aliphatic amines containing two or more nitrogen atoms by preparing carbamate salts in situ even under ambient conditions.

Chemistry LettersVol. 54(2)
Industrial Technology Center of Okayama Prefecture (JP)
Openalex Percentile: Top 40%
Carbon dioxide utilization in catalysis
0.70
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