An original one-pot approach to boronic esters using the titanium-catalyzed reaction of cyclic olefins with alkyldichloroboranes

Publication date: Available online 17 July 2018Source: Journal of Organometallic ChemistryAuthor(s): Liliya I. Khusainova, Leila O. Khafizova, Tatyana V. Tyumkina, Kirill S. Ryazanov, Natalya R. Popodko, Usein M. DzhemilevAbstractBoronic esters (dicycloheptylalkylboronates, dicyclooctylalkylboronates, dicyclododecylalkylboronates, dibicyclo[2.2.1]hept-2-ylalkylboronates) are produced with yields ranging from moderate to excellent (52–96%) by the reaction between cyclic olefins (cycloheptene, cis-cyclooctene, cis/trans-cyclododecene, norbornene) and alkyldichloroboranes (alkyl = Et, n-Pent) in the presence of metallic magnesium and the Cp2TiCl2 catalyst with subsequent addition of water.Graphical abstract
Source: Journal of Organometallic Chemistry - Category: Chemistry Source Type: research
More News: Chemistry | Magnesium