Palladium-Catalyzed\nCross-Coupling of Aryl Bromides\nand Chlorides with Trimethylsilylalkynes under Mild Conditions

Herein, we disclose a palladium-catalyzed\ncross-coupling\nof aryl\nbromides and chlorides with trimethylsilylalkynes under mild reaction\nconditions. This method utilizes commercially available and air stable\npalladium precatalysts and avoids the use of copper cocatalysts. Moreover,\nit allows for the synthesis of a wide range of disubstituted alkynes\nin high yields with excellent functional group tolerance. The utility\nof the developed method was further demonstrated via the late-stage\nalkynylation of pharmaceuticals and natural bioactive compounds.

Publication Details

Journal
Figshare
Published
2024-09-02
DOI
https://doi.org/10.1021/acs.joc.4c01499.s001
Primary Topic
Education Methods and Technologies
Type
article
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article

Palladium-Catalyzed\nCross-Coupling of Aryl Bromides\nand Chlorides with Trimethylsilylalkynes under Mild Conditions

Figshare
Education Methods and Technologies
article

Palladium-Catalyzed\nCross-Coupling of Aryl Bromides\nand Chlorides with Trimethylsilylalkynes under Mild Conditions

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Abstract

Herein, we disclose a palladium-catalyzed\ncross-coupling\nof aryl\nbromides and chlorides with trimethylsilylalkynes under mild reaction\nconditions. This method utilizes commercially available and air stable\npalladium precatalysts and avoids the use of copper cocatalysts. Moreover,\nit allows for the synthesis of a wide range of disubstituted alkynes\nin high yields with excellent functional group tolerance. The utility\nof the developed method was further demonstrated via the late-stage\nalkynylation of pharmaceuticals and natural bioactive compounds.

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Education Methods and Technologies
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Palladium-Catalyzed\nCross-Coupling of Aryl Bromides\nand Chlorides with Trimethylsilylalkynes under Mild Conditions · Figshare (2024) | TGRS Research Map | TGRS