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- W2090609208 abstract "An efficient and practical copper-catalyzed highly regio- and stereoselective borylcupration of internal alkynes with bis(pinacolato)diboron using a catalytic amount of K2CO3 as base producing Z-alkenylboron compounds has been demonstrated by applying the ligand effect: commercially available electron-rich tris(p-methoxyphenyl) phosphine ensures a smooth and efficient reaction. Functionalized alkynes, such as propargylic alcohols and derivatives as well as N-propargyl tosylamide, may also be used with excellent selectivity." @default.
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- W2090609208 date "2012-01-01" @default.
- W2090609208 modified "2023-10-07" @default.
- W2090609208 title "CuCl–K2CO3-catalyzed highly selective borylcupration of internal alkynes – ligand effect" @default.
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- W2090609208 doi "https://doi.org/10.1039/c2ob26147b" @default.
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