We reveal {here|right here} the regioselective nucleophilic addition of C(sp3) to 1,1-arylboryl alkenes, followed by nucleophilic attack {of the|from the|in the|on the|with the|of your} alpha-boryl carbanionic intermediates to C(sp3) electrophiles, at {room|space|area} temperature. We envisioned this {goal|objective|aim|purpose|target} {through|via|by means of|by way of} engaged C(sp3) chemical entities avoiding metal catalysts, additives, radical initiators or {specific|particular|certain|distinct|precise} irradiation. This multicomponent reaction guarantees that the new tetrasubstituted carbon formed retains {all the|all of the|each of the} C atoms {from the|in the} {three|3} {starting|beginning} {materials|supplies|components} involved {in the|within the|inside the} assembly. 3,5-Dibromo-1H-pyrazole-4-carbonitrile Data Sheet Buy1-(2-Hydroxy-5-iodophenyl)ethan-1-one PMID:24624203
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