Magnesiation Employing Grignard Reagents and Catalytic Amine. Application to the Functionalization of <i>N</i>-Phenylsulfonylpyrrole

Andrew Dinsmore, D.G. Billing, Karen Mandy, Joseph P. Michael, Daniel Mogano, Shivaputra A. Patil

Organic Letters · 2003 · 31 citations · 8 references

Concepts

Abstract

[reaction: see text] N-Phenylsulfonylpyrrole 1 is magnesiated by treatment with isopropylmagnesium chloride and catalytic diisopropylamine. Reaction with various electrophiles, including palladium-catalyzed aryl- and heteroaryl cross-coupling, provides 2-substituted phenylsulfonylpyrroles in moderate to good yields.

References

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