Highly selective α-C(sp3)-H arylation of alkenyl amides via nickel chain-walking catalysis

Shi, Haoran; Wang, Jiaxin; Zhu, Yuqin; Li, Hongyang; Ju, Guodong; Zhang, Lanlan; Wang, Chao

doi:10.1016/j.cclet.2023.109333

Chinese Chemical Letters

2024

DOI: 10.1016/j.cclet.2023.109333

|View full text |Cite

Highly selective α-C(sp3)-H arylation of alkenyl amides via nickel chain-walking catalysis

Haoran Shi,

Jiaxin Wang,

Yuqin Zhu

et al.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2024

Publication Types

Select...

Article2

Relationship

Self Cite0

Independent2

Authors

Journals

Cited by 2 publications

References 78 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

Cobalt‐Catalyzed Hydroarylation of 2,3‐Dihydrofuran to Access α‐Arylated Tetrahydrofurans

Sun,

Lu,

2024

ChemCatChem

View full text Add to dashboard Cite

α‐Arylated tetrahydrofurans, commonly found in biologically active molecules, exhibit diverse biologically activities and pharmacological effects. The functionalization of 2,3‐dihydrofuran offers a potential route for the synthesis of substituted tetrahydrofurans. Nevertheless, the development of earth‐abundant metal‐catalyzed regioselective hydrofunctionalization of 2,3‐dihydrofuran for the synthesis of substituted tetrahydrofurans remains to be pursued. Herein, we report a cobalt‐catalyzed hydroarylation of 2,3‐dihydrofuran, which serves as the first example of cobalt‐hydride‐catalyzed alkene hydroarylation. This reaction provides an efficient method for the synthesis of α‐arylated tetrahydrofurans with high reaction efficiency, exclusive α‐arylation selectivity, and remarkable functional group compatibility.

show abstract

Cobalt‐Catalyzed Hydroarylation of 2,3‐Dihydrofuran to Access α‐Arylated Tetrahydrofurans

Sun,

Lu,

2024

ChemCatChem

View full text Add to dashboard Cite

show abstract

Coordination-Assisted Ni-Catalyzed Regio- and Enantioselective 1,2-Borylalkylation of Unactivated Alkenes

Zhu,

Feng,

et al. 2024

Org. Lett.

View full text Add to dashboard Cite

show abstract

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Highly selective α-C(sp3)-H arylation of alkenyl amides via nickel chain-walking catalysis

Cited by 2 publications

References 78 publications

Cobalt‐Catalyzed Hydroarylation of 2,3‐Dihydrofuran to Access α‐Arylated Tetrahydrofurans

Cobalt‐Catalyzed Hydroarylation of 2,3‐Dihydrofuran to Access α‐Arylated Tetrahydrofurans

Coordination-Assisted Ni-Catalyzed Regio- and Enantioselective 1,2-Borylalkylation of Unactivated Alkenes

Contact Info

Product

Resources

About