Synthesis of Tetrahydroisoquinolinoquinolines via Sequential Pd-Catalyzed N-Arylation and Pd-Catalyzed Alkene Carboamination Reactions

Abstract The synthesis of substituted tetrahydroisoquinolinoquinolines via a two-step route involving a Pd-catalyzed N-arylation reaction followed by a Pd-catalyzed alkene carboamination reaction is described. The combined transformations lead to the generation of two rings and three bonds (two C–N and one C–C) and the heterocyclic products are obtained in moderate to good yields.

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Publication Details

Journal
Synthesis
Published
2026-01-20
DOI
https://doi.org/10.1055/a-2759-6397
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
22.95
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article

Synthesis of Tetrahydroisoquinolinoquinolines via Sequential Pd-Catalyzed N-Arylation and Pd-Catalyzed Alkene Carboamination Reactions

Gabriel González, John P. Wolfe, Glorimar Miranda-Mendez, Kathryn G. Berges
1 citations
Synthesis
Catalytic C–H Functionalization Methods
22.95
article

Synthesis of Tetrahydroisoquinolinoquinolines via Sequential Pd-Catalyzed N-Arylation and Pd-Catalyzed Alkene Carboamination Reactions

Gabriel González, John P. Wolfe, Glorimar Miranda-Mendez, Kathryn G. Berges
article en
1 citations

Abstract

Abstract The synthesis of substituted tetrahydroisoquinolinoquinolines via a two-step route involving a Pd-catalyzed N-arylation reaction followed by a Pd-catalyzed alkene carboamination reaction is described. The combined transformations lead to the generation of two rings and three bonds (two C–N and one C–C) and the heterocyclic products are obtained in moderate to good yields.

Synthesis
University of Michigan (US)
Openalex Percentile: Top 2%
Catalytic C–H Functionalization Methods
22.95
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