A masked diboron in Cu-catalysed borylation reaction: highly regioselective formal hydroboration of alkynes for synthesis of branched alkenylborons?
Chemical Communications Pub Date: 2014-04-08 DOI: 10.1039/C4CC01757A
Abstract
The use of a masked diboron as a boron source in the presence of a Cu–N-heterocyclic carbene (NHC) catalyst enables alkyl-, aryl-, heteroatom- and silyl-substituted terminal alkynes to undergo α-selective formal hydroboration to give diverse branched alkenylboron compounds exclusively. Synthetic potential of this α-selective hydroboration has been demonstrated by total synthesis of pharmaceutically significant bexarotene and LG100268.
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Journal Name:Chemical Communications
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CAS no.: 89640-58-4