Ruthenium-catalyzed C-H amination of aroylsilanes.

Org Biomol Chem

College of Materials, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 311121, China. and Department of Stomatology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou, 310015, China.

Published: July 2021

Acylsilane represents a valuable synthon in synthetic chemistry. We report on ruthenium(ii)-catalyzed ortho-C-H amination of aroylsilanes to provide facile access to synthetically useful imidobenzoylsilanes and tosyl-amidobenzoylsilanes. The protocols, with broad substrate scope and excellent functional group tolerance, are enabled with the weak chelation-assistance of acylsilane via C-H cyclometallation.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d1ob00935dDOI Listing

Publication Analysis

Top Keywords

amination aroylsilanes
8
ruthenium-catalyzed c-h
4
c-h amination
4
aroylsilanes acylsilane
4
acylsilane represents
4
represents valuable
4
valuable synthon
4
synthon synthetic
4
synthetic chemistry
4
chemistry report
4

Similar Publications

Ruthenium-catalyzed C-H amination of aroylsilanes.

Org Biomol Chem

July 2021

College of Materials, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 311121, China. and Department of Stomatology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou, 310015, China.

Acylsilane represents a valuable synthon in synthetic chemistry. We report on ruthenium(ii)-catalyzed ortho-C-H amination of aroylsilanes to provide facile access to synthetically useful imidobenzoylsilanes and tosyl-amidobenzoylsilanes. The protocols, with broad substrate scope and excellent functional group tolerance, are enabled with the weak chelation-assistance of acylsilane via C-H cyclometallation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!