《Boronic acid-mediated ring-opening and Ni-catalyzed arylation of 1-arylcyclopropyl tosylates》 was written by Mills, L. Reginald; Monteith, John J.; Rousseaux, Sophie A. L.. Category: chlorides-buliding-blocks And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2020. The article conveys some information:
The ring-opening arylation of 1-arylcyclopropyl tosylates, in which boronic acids promoted ring-opening and a Ni catalyst facilitated arylation in high regioselectivity was described. A number of 2-arylated allyl derivatives were synthesized, which are relevant motifs found in biol. active mols. The experimental part of the paper was very detailed, including the reaction process of (3-Fluorophenyl)boronic acid(cas: 768-35-4Category: chlorides-buliding-blocks)
(3-Fluorophenyl)boronic acid(cas: 768-35-4) can be used to make novel liquid crystalline fluorobiphenylcyclohexenes and difluoroterphenyls by palladium-catalyzed cross-couplings also used in the synthesis of o-phenylphenols as potent leukotriene B4 receptor agonists.Category: chlorides-buliding-blocks
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics