Amanote Research

Amanote Research

    RegisterSign In

Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group

doi 10.1021/acs.joc.9b01563.s002
Full Text
Open PDF
Abstract

Available in full text

Date

Unknown

Authors

Unknown

Publisher

American Chemical Society (ACS)


Related search

Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group

English

Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group

English

Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group

English

Palladium-Catalyzed Site-Selective Sp3 CH Bond Thiocyanation of 2Aminofurans

English

Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations

English

Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations

English

Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations

English

Pd-Catalyzed, Ortho CH Methylation and Fluorination of Benzaldehydes Using Orthanilic Acids as Transient Directing Groups

English

Ruthenium Catalyzed CH Selenylations of Aryl Acetic Amides and Esters via Weak Coordination

English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy