B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>‑Catalyzed\nMulticomponent Reactions of 2,3-Diketoesters, Amines, Allenes, and\nNucleophiles: Synthesis of 2α-Functionalized Pyrroles

An efficient B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-catalyzed\nmulticomponent reaction of 2,3-diketoesters, amines, allenes, and\nnucleophiles was reported, which afforded 2α-functionalized\npyrroles in moderate to good yields. The reaction features low catalyst\nloading, usage of a small amount of solvent, high atom economy, tunable\ninstallation of diverse functional groups at 2α-position, and\nwater being formed as the byproduct. This is the first multicomponent\nreaction that combines vicinal tricarbonyl compounds with allenes.

Publication Details

Journal
Figshare
Published
2024-08-15
DOI
https://doi.org/10.1021/acs.joc.4c01221.s001
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
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article

B(C6F5)3‑Catalyzed\nMulticomponent Reactions of 2,3-Diketoesters, Amines, Allenes, and\nNucleophiles: Synthesis of 2α-Functionalized Pyrroles

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Synthesis and Characterization of Pyrroles
article

B(C6F5)3‑Catalyzed\nMulticomponent Reactions of 2,3-Diketoesters, Amines, Allenes, and\nNucleophiles: Synthesis of 2α-Functionalized Pyrroles

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Abstract

An efficient B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-catalyzed\nmulticomponent reaction of 2,3-diketoesters, amines, allenes, and\nnucleophiles was reported, which afforded 2α-functionalized\npyrroles in moderate to good yields. The reaction features low catalyst\nloading, usage of a small amount of solvent, high atom economy, tunable\ninstallation of diverse functional groups at 2α-position, and\nwater being formed as the byproduct. This is the first multicomponent\nreaction that combines vicinal tricarbonyl compounds with allenes.

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Synthesis and Characterization of Pyrroles
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B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>‑Catalyzed\nMulticomponent Reactions of 2,3-Diketoesters, Amines, Allenes, and\nNucleophiles: Synthesis of 2α-Functionalized Pyrroles · Figshare (2024) | TGRS Research Map | TGRS