Synthesis of 2,4,5-vinylic-trisubstituted oxazoles via a Palladium-catalyzed cascade coupling reaction

A novel cascade coupling approach to the assembly of 2,4,5-vinyl-trisubstituted oxazoles is described. This reaction employs readily accessible β,β-dibrominated secondary enamides and terminal alkenes , and proceeds via a ligand-free Pd-catalyzed cascade C O coupling/Heck reaction. A novel one-step synthesis of valuable 2,4,5-vinylic-trisubstituted oxazoles is described. This reaction, utilizing readily available β,β-dibrominated secondary enamides and terminal alkenes as starting materials, occurs via a ligand-free Palladium-catalyzed cascade intramolecular C O coupling/intermolecular Heck reaction .

Authors

Publication Details

Journal
Tetrahedron Letters
Published
2024-11-21
DOI
https://doi.org/10.1016/j.tetlet.2024.155373
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.00
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article

Synthesis of 2,4,5-vinylic-trisubstituted oxazoles via a Palladium-catalyzed cascade coupling reaction

Qingyu Meng, Jun Ma, Zheng Li, Fangyi Li et al.
4 citations
Tetrahedron Letters
Catalytic C–H Functionalization Methods
1.00
article

Synthesis of 2,4,5-vinylic-trisubstituted oxazoles via a Palladium-catalyzed cascade coupling reaction

Qingyu Meng, Jun Ma, Zheng Li, Fangyi Li, Huali Wang, Haoyue Wang
article en
4 citations

Abstract

A novel cascade coupling approach to the assembly of 2,4,5-vinyl-trisubstituted oxazoles is described. This reaction employs readily accessible β,β-dibrominated secondary enamides and terminal alkenes , and proceeds via a ligand-free Pd-catalyzed cascade C O coupling/Heck reaction. A novel one-step synthesis of valuable 2,4,5-vinylic-trisubstituted oxazoles is described. This reaction, utilizing readily available β,β-dibrominated secondary enamides and terminal alkenes as starting materials, occurs via a ligand-free Palladium-catalyzed cascade intramolecular C O coupling/intermolecular Heck reaction .

Tetrahedron LettersVol. 153
Openalex Percentile: Top 26%
Catalytic C–H Functionalization Methods
1.00
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