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Iridium-catalyzed conversion of alcohols into amides via oximes.

Organic letters (2006-12-29)
Nathan A Owston, Alexandra J Parker, Jonathan M J Williams
ABSTRACT

[reaction: see text] The iridium catalyst [Ir(Cp*)Cl2]2 is effective for the rearrangement of oximes to furnish amides. The reaction has been combined with catalytic transfer hydrogenation between an alcohol and alkene to allow the conversion of alcohols into amides in a one-pot process.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,2,3,4,5-Pentamethylcyclopentadiene, 95%