The borylation of an aryl halide or aryl triflate with a boron source, typically a boronic ester, is the initial step. Common reagents include B2pin2 (bis(pinacolato)diboron) or BBr3. The choice of boron source depends on the specific reaction conditions and substrate.
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2-methyl-5-nitro-1-tosyl-1H-indole
(2-bromoethenylidene)cyclohexane
methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(2,4,5-trifluorophenyl)-butanoate
2-(pinacolboryl)-4-phenylfuran
3'-(Methoxycarbonyl)biphenyl-4-boronic acid pinacol ester, 95%
potassium trifluoro(2-methylbenzoyl)borate
