Electrochemical Nickel-Catalyzed 1,2-Diarylation of 1,3-Dienes

Chen, Wangzhe; Yu, Lei; Pan, Yi; Ni, Shengyang; Wang, Yi

doi:10.1021/acs.orglett.3c03936

Org. Lett.

2023

DOI: 10.1021/acs.orglett.3c03936

|View full text |Cite

Electrochemical Nickel-Catalyzed 1,2-Diarylation of 1,3-Dienes

Wangzhe Chen,

Lei Yu,

Yi Pan

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...

Article3

Relationship

Self Cite0

Independent3

Authors

Journals

Cited by 3 publications

(1 citation statement)

References 63 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…8 Therefore, the previous work by Wang, Tang, Lee, and other groups also concentrated on the synthesis of valuable thioether derivatives by utilizing aryl alkenes, amines, and arynes as the coupling partners. 9 Unfortunately, the C–H thioetheration of hydrazones has not been reported.…”

mentioning

confidence: 99%

Electrochemical oxidative thioetherification of aldehyde hydrazones with thiophenols

Hu,

Yang,

Zhang

et al. 2024

Org. Biomol. Chem.

View full text Add to dashboard Cite

show abstract

mentioning

confidence: 99%

Electrochemical oxidative thioetherification of aldehyde hydrazones with thiophenols

Hu,

Yang,

Zhang

et al. 2024

Org. Biomol. Chem.

View full text Add to dashboard Cite

show abstract

Regio- and Stereoselective Electro-Mediated Carboalkoxylation of 1,3-Dienes

Montiège,

Siccardi,

Sanselme

et al. 2024

Org. Lett.

View full text Add to dashboard Cite

A review of recent advances in electrochemical and photoelectrochemical late-stage functionalization classified by anodic oxidation, cathodic reduction, and paired electrolysis

Li,

Sitdikov,

Kale

et al. 2024

Beilstein J. Org. Chem.

View full text Add to dashboard Cite

With the resurgence of electrosynthesis in organic chemistry, there is a significant increase in the number of routes available for late-stage functionalization (LSF) of drugs. Electrosynthetic methods, which obviate the need for hazardous chemical oxidants or reductants, offer unprecedented control of reactions through the continuous variation of the applied potential and the possibility of combination with photochemical processes. This capability is a substantial advantage for performing electrochemical or photoelectrochemical LSF. Ultimately, these protocols are poised to become a vital component of the medicinal chemist's toolkit. In this review, we discuss electrochemical protocols that have been demonstrated to be applicable for the LSF of pharmaceutical drugs, their derivatives, and natural substrates. We present and analyze representative examples to illustrate the potential of electrochemistry or photoelectrochemistry for the LSF of valuable molecular scaffolds.

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.

Electrochemical Nickel-Catalyzed 1,2-Diarylation of 1,3-Dienes

Cited by 3 publications

References 63 publications

Electrochemical oxidative thioetherification of aldehyde hydrazones with thiophenols

Electrochemical oxidative thioetherification of aldehyde hydrazones with thiophenols

Regio- and Stereoselective Electro-Mediated Carboalkoxylation of 1,3-Dienes

A review of recent advances in electrochemical and photoelectrochemical late-stage functionalization classified by anodic oxidation, cathodic reduction, and paired electrolysis

Contact Info

Product

Resources

About