Title of article :
In situ formation and reaction of 2-pyridylboronic esters
Author/Authors :
Fuller، نويسنده , , Amelia A and Hester، نويسنده , , Heidi R and Salo، نويسنده , , Eric V and Stevens، نويسنده , , Erland P، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
4
From page :
2935
To page :
2938
Abstract :
2-Pyridylboronic esters were generated by cross-coupling 2-bromopyridines with bis(pinacolato)diboron in the presence of a base and palladium catalyst. The boronic esters reacted in situ with unreacted 2-bromopyridines to afford high yields of 2,2′-bipyridines as homocoupled products. Depending upon the reaction conditions, varying amounts of protodeboronated products were also observed. An attempted cross-coupling between two different 2-bromopyridines produced a nearly statistical mixture of homo- and cross-coupled products.
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1661563
Link To Document :
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