Highly regio-selective hydration of ynamides under catalyst-free conditions

The highly regio-selective hydration of ynamides under catalyst-free conditions has been demonstrated for easily accessing α-amidoketones in 51-99% yields. The excellent regio-selectivity is believed to be controlled by the amide group, which is just opposite to that observed in Brønsted acid-mediated hydration of ynamides. This approach is highly convenient, easy to operate, and exhibits good functionality tolerance.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00581g
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Highly regio-selective hydration of ynamides under catalyst-free conditions

Peng Bao, Yeqing Wang, Qiuwen Li, Han Xiao et al.
1 citations
Organic & Biomolecular Chemistry
Catalytic Alkyne Reactions
0.94
article

Highly regio-selective hydration of ynamides under catalyst-free conditions

Peng Bao, Yeqing Wang, Qiuwen Li, Han Xiao, Gang He, Yi Wang
article en
1 citations

Abstract

The highly regio-selective hydration of ynamides under catalyst-free conditions has been demonstrated for easily accessing α-amidoketones in 51-99% yields. The excellent regio-selectivity is believed to be controlled by the amide group, which is just opposite to that observed in Brønsted acid-mediated hydration of ynamides. This approach is highly convenient, easy to operate, and exhibits good functionality tolerance.

Organic & Biomolecular ChemistryVol. 23(24)
Nanjing Tech University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 26%
Catalytic Alkyne Reactions
0.94
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