Palladium-Catalyzed Regio- and Diastereoselective Hydro(hetero)arylation for Rapid Construction of Quaternary Center Containing Cyclobutanes

Herein we report a Pd-catalyzed regio- and diastereoselective hydro(hetero)arylation of inactivated alkylidenecyclobutanes. This protocol provides a rapid and atom-economical route to access 3-cyclobutyl (hetero)arenes with good functionalities toleration. With the assistance of the directing group, nucleophilic attack happened on the bulkier γ-position to form the quaternary carbon center. Furthermore, the selected products exhibited antitumor bioactivities.

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Publication Details

Journal
Organic Letters
Published
2024-08-19
DOI
https://doi.org/10.1021/acs.orglett.4c02645
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.50

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article

Palladium-Catalyzed Regio- and Diastereoselective Hydro(hetero)arylation for Rapid Construction of Quaternary Center Containing Cyclobutanes

Jia Zheng, Mandalaparthi Phanindrudu, Shuaikang Li, Hui Luo et al.
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
0.50
article

Palladium-Catalyzed Regio- and Diastereoselective Hydro(hetero)arylation for Rapid Construction of Quaternary Center Containing Cyclobutanes

Jia Zheng, Mandalaparthi Phanindrudu, Shuaikang Li, Hui Luo, Yi Qi, Furong Tao, Haifei Yang
article en
2 citations

Abstract

Herein we report a Pd-catalyzed regio- and diastereoselective hydro(hetero)arylation of inactivated alkylidenecyclobutanes. This protocol provides a rapid and atom-economical route to access 3-cyclobutyl (hetero)arenes with good functionalities toleration. With the assistance of the directing group, nucleophilic attack happened on the bulkier γ-position to form the quaternary carbon center. Furthermore, the selected products exhibited antitumor bioactivities.

Organic LettersVol. 26(34)
Guangdong Medical College (CN), Marine Biomedical Research Institute of Qingdao (CN)
Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 40%
Catalytic C–H Functionalization Methods
0.50
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