A Mild and Regioselective Method for -Bromination of align="midd
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Bromodimethylsulfonium bromide has been found to be aneffective and regioselective reagent for -monobrominationof -keto esters and 1,3-diketones. A wide variety of -ketoesters and 1,3-diketones undergo chemoselective -monobromination with excellent yields at 0-5 C or roomtemperature. The notable advantages of this protocol are noneed of chromatographic separation, use of less hazardousreagent than molecular bromine, and no added base, Lewisacid, or other catalyst.

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