Literature DB >> 12919061

Application of the Suzuki reaction as the key step in the synthesis of a novel atropisomeric biphenyl derivative for use as a liquid crystal dopant.

Andrew N Cammidge1, Karen V L Crépy.   

Abstract

A heavily functionalized atropisomeric biphenyl derivative (4), which is designed to possess a large lateral dipole moment, has been synthesized with use of a Suzuki coupling as the key step and resolved by chiral HPLC. The final coupling reaction is complicated by rapid hydrolytic deboronation of the sterically hindered, electron poor boronate 22. Rigorously anhydrous conditions are therefore necessary to achieve the coupling.

Entities:  

Year:  2003        PMID: 12919061     DOI: 10.1021/jo034652s

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

1.  Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki-Miyaura Cross-Coupling of Boronic Esters.

Authors:  Connor P Delaney; Vincent M Kassel; Scott E Denmark
Journal:  ACS Catal       Date:  2019-12-02       Impact factor: 13.084

2.  Heteroaryl-Heteroaryl, Suzuki-Miyaura, Anhydrous Cross-Coupling Reactions Enabled by Trimethyl Borate.

Authors:  Vincent M Kassel; Christopher M Hanneman; Connor P Delaney; Scott E Denmark
Journal:  J Am Chem Soc       Date:  2021-08-20       Impact factor: 16.383

3.  In Situ Studies of Arylboronic Acids/Esters and R3SiCF3 Reagents: Kinetics, Speciation, and Dysfunction at the Carbanion-Ate Interface.

Authors:  Andrés García-Domínguez; Andrew G Leach; Guy C Lloyd-Jones
Journal:  Acc Chem Res       Date:  2022-04-18       Impact factor: 24.466

4.  Asymmetric Oxidative Coupling of Phenols and Hydroxycarbazoles.

Authors:  Houng Kang; Young Eun Lee; Peddiahgari Vasu Govardhana Reddy; Sangeeta Dey; Scott E Allen; Kyle A Niederer; Paul Sung; Kirsten Hewitt; Carilyn Torruellas; Madison R Herling; Marisa C Kozlowski
Journal:  Org Lett       Date:  2017-10-12       Impact factor: 6.005

  4 in total

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