Metal-free Borylation of α-Naphthamides and Phenylacetic Acid Drug-Reference-Cited by-同舟云学术

Metal-free Borylation of α-Naphthamides and Phenylacetic Acid Drug

Published:2024-09-11 Issue: Volume: Page:
ISSN:2691-3704
Container-title:JACS Au
language:en
Short-container-title:JACS Au

Author:

Maji Suman¹,Rawal Parveen²^ORCID,Ghosh Animesh¹,Pidiyar Karishma¹,Al-Thabaiti Shaeel A.³,Gupta Puneet²⁴^ORCID,Maiti Debabrata¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India

2. Computational Catalysis Center, Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India

3. Department of Chemistry, Faculty of Science, King Abdulaziz University institution, P.O. Box : 80203, Jeddah, 21589, Saudi Arabia

4. Department of Chemistry, Faculty of ScienceCenter for Sustainable Energy, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India

Funder

King Abdulaziz University

Ministry of Education - Kingdom of Saudi Arabia

Institutional Fund Project

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacsau.4c00660

Reference63 articles.

1. Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters

2. A Stoichiometric Aromatic CH Borylation Catalyzed by Iridium( I )/2,2′‐Bipyridine Complexes at Room Temperature

3. Regioselective Borylation of Porphyrins by CH Bond Activation under Iridium Catalysis to Afford Useful Building Blocks for Porphyrin Assemblies

4. Regioselectivity of the borylation of alkanes and arenes

5. A meta-selective C–H borylation directed by a secondary interaction between ligand and substrate