Novel Kumada Coupling Reaction to Access Cyclic (2-Azaallyl) stannanes. Cycloadditions of Cyclic Nonstabilized 2-Azaallyllithium Species Derived from Cyclic (2- …
DM Mans, WH Pearson
Index: Mans, Douglas M.; Pearson, William H. Journal of Organic Chemistry, 2004 , vol. 69, # 19 p. 6419 - 6426
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Citation Number: 12
Abstract
A Kumada cross-coupling reaction involving organomagnesium reagents and (3-methylthio- 2-azaallyl) stannanes with a Ni (0) catalyst provided cyclic nonstabilized (2-azaallyl) stannanes in moderate to good yields. Primary alkyl, aryl, and allylic organomagnesium reagents can be used as the cross-coupling partner. In general, NiCl2dppp in toluene at room temperature provided the shortest reaction times and most consistent yields. The ...
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