Nickel-Catalyzed\nNarasaka–Heck Cyclization\nCarbonylation of Unsaturated Oxime Esters with Arylboronic Acids

The Narasaka–Heck reaction is one of the most\nstraightforward\nmethods for constructing pyrroline derivatives. Herein, we report\na novel nickel-catalyzed three-component carbonylation reaction, which\ncleverly realizes the continuous construction of C(sp<sup>3</sup>)–N\nbonds and C(sp<sup>3</sup>)–C(sp<sup>2</sup>) bonds and effectively\npromotes the synthesis of acyl-substituted pyrroline derivatives.\nFurthermore, this strategy not only expands the conversion pathway\nof γ,δ-unsaturated oxime esters but also provides a new\nmethod for the synthesis of nitrogen-containing heterocyclic compounds.

Publication Details

Journal
Figshare
Published
2024-09-05
DOI
https://doi.org/10.1021/acs.orglett.4c02647.s001
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Nickel-Catalyzed\nNarasaka–Heck Cyclization\nCarbonylation of Unsaturated Oxime Esters with Arylboronic Acids

Figshare
Catalytic Cross-Coupling Reactions
article

Nickel-Catalyzed\nNarasaka–Heck Cyclization\nCarbonylation of Unsaturated Oxime Esters with Arylboronic Acids

article en

Abstract

The Narasaka–Heck reaction is one of the most\nstraightforward\nmethods for constructing pyrroline derivatives. Herein, we report\na novel nickel-catalyzed three-component carbonylation reaction, which\ncleverly realizes the continuous construction of C(sp<sup>3</sup>)–N\nbonds and C(sp<sup>3</sup>)–C(sp<sup>2</sup>) bonds and effectively\npromotes the synthesis of acyl-substituted pyrroline derivatives.\nFurthermore, this strategy not only expands the conversion pathway\nof γ,δ-unsaturated oxime esters but also provides a new\nmethod for the synthesis of nitrogen-containing heterocyclic compounds.

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Catalytic Cross-Coupling Reactions
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Nickel-Catalyzed\nNarasaka–Heck Cyclization\nCarbonylation of Unsaturated Oxime Esters with Arylboronic Acids · Figshare (2024) | TGRS Research Map | TGRS