Tunable mono- or 1,1-double Heck-type coupling reaction of unconjugated amido-alkenes with remote benzylic C(sp <sup>3</sup> )–H of <i>N</i> -fluorobenzamides

A tunable mono- or unprecedented 1,1-double Heck-type cross-coupling of unconjugated amido-alkenes directed by the remote C(sp 3 )–H of N -fluorobenzamides was developed, and a variety of polysubstituted alkenes was obtained in good yields.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2024-12-11
DOI
https://doi.org/10.1039/d4qo01971g
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.50
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article

Tunable mono- or 1,1-double Heck-type coupling reaction of unconjugated amido-alkenes with remote benzylic C(sp 3 )–H of N -fluorobenzamides

Tianyu Lu, Weixing Chang, Lingyan Liu, Jing Li
2 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
0.50
article

Tunable mono- or 1,1-double Heck-type coupling reaction of unconjugated amido-alkenes with remote benzylic C(sp 3 )–H of N -fluorobenzamides

Tianyu Lu, Weixing Chang, Lingyan Liu, Jing Li
article en
2 citations

Abstract

A tunable mono- or unprecedented 1,1-double Heck-type cross-coupling of unconjugated amido-alkenes directed by the remote C(sp 3 )–H of N -fluorobenzamides was developed, and a variety of polysubstituted alkenes was obtained in good yields.

Organic Chemistry FrontiersVol. 12(4)
Nankai University (CN), Collaborative Innovation Center of Chemical Science and Engineering Tianjin (CN)
Openalex Percentile: Top 37%
Catalytic C–H Functionalization Methods
0.50
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