| Literature DB >> 25959852 |
James W B Fyfe1, Elena Valverde2, Ciaran P Seath1, Alan R Kennedy1, Joanna M Redmond3, Niall A Anderson3, Allan J B Watson4.
Abstract
Boronic acid solution speciation can be controlled during the Suzuki-Miyaura cross-coupling of haloaryl N-methyliminodiacetic acid (MIDA) boronic esters to enable the formal homologation of boronic acid derivatives. The reaction is contingent upon control of the basic biphase and is thermodynamically driven: temperature control provides highly chemoselective access to either BMIDA adducts at room temperature or boronic acid pinacol ester (BPin) products at elevated temperature. Control experiments and solubility analyses have provided some insight into the mechanistic operation of the formal homologation process.Entities:
Keywords: boron; chemoselectivity; cross-coupling; palladium; speciation
Mesh:
Substances:
Year: 2015 PMID: 25959852 DOI: 10.1002/chem.201500970
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236