Highly regio- and stereoselective synthesis of alkenylboronic esters by copper-catalyzed boron additions to disubstituted alkynes

The copper-catalyzed addition of bis(pinacolato)diboron to internal alkynes in the presence of methanol generates alkenylboron compounds with high levels of regio- and stereoselectivities. The catalytic efficiency is increased by using monodentate phosphine ligands, especially P(p-tolyl)(3) and a ra...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2011-01, Vol.47 (10), p.2943-2945
Hauptverfasser: Kim, Hye Ryung, Yun, Jaesook
Format: Artikel
Sprache:eng
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Zusammenfassung:The copper-catalyzed addition of bis(pinacolato)diboron to internal alkynes in the presence of methanol generates alkenylboron compounds with high levels of regio- and stereoselectivities. The catalytic efficiency is increased by using monodentate phosphine ligands, especially P(p-tolyl)(3) and a range of internal alkynes was borylated in good yields.
ISSN:1359-7345
1364-548X
DOI:10.1039/c0cc04496b