Journal
DALTON TRANSACTIONS
Volume -, Issue 8, Pages 1055-1064Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b715584k
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We present herein a high yield, highly selective catalytic synthesis of vinylboronate esters (VBEs), including 1,1-disubstituted VBEs, from alkenes without significant hydrogenation or hydroboration, using the simple catalyst precursor, trans-[RhCl(CO)(PPh3)(2)] (1), and the diboron reagents B(2)pin(2) (2a, pin = pinacolato = OCMe2CMe2O) or B(2)neop(2) (2b, neop = neopentylglycolato = OCH2CMe2CH2O), or the monoboron reagent HBpin, all of which are commercially available. The reactions were conducted at 80 degrees C using conventional heating, or in a microwave reactor at 150 degrees C.
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