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Ring expansions of acyloxy nitroso compounds.

ABSTRACT: Treatment of cyclopentanone and cyclobutanone-derived oximes with lead (IV) tetraacetate gives the bright blue acyloxy nitroso compounds, which upon basic hydrolysis yields the ring expansion product cyclic hydroxamic acids in 12-81% yield. Reactions of substituted cyclopentanones provide ring expanded products where the -NOH group regioselectively inserts to the more substituted position and gives a better yield compared to the treatment of the same ketone with a basic solution of Piloty's acid. Reaction of phosphines with acyloxy nitroso compounds generally generates a ring-expanded Beckmann rearrangement product that can be hydrolyzed to the corresponding lactam. Acyloxy nitroso compounds that undergo rapid hydrolysis to HNO do not show this ring expansion reactivity. These results further demonstrate the versatility of acyloxy nitroso compound to yield structurally complex materials.

SUBMITTER: Hadimani MB

PROVIDER: S-EPMC4671303 | biostudies-literature | 2015 Oct

REPOSITORIES: biostudies-literature

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Ring expansions of acyloxy nitroso compounds.

Hadimani Mallinath B MB Mukherjee Rajeswari R Banerjee Ranjan R Shoman Mai E ME Aly Omar M OM King S Bruce SB

Tetrahedron letters 20151001 43

Treatment of cyclopentanone and cyclobutanone-derived oximes with lead (IV) tetraacetate gives the bright blue acyloxy nitroso compounds, which upon basic hydrolysis yields the ring expansion product cyclic hydroxamic acids in 12-81% yield. Reactions of substituted cyclopentanones provide ring expanded products where the -NOH group regioselectively inserts to the more substituted position and gives a better yield compared to the treatment of the same ketone with a basic solution of Piloty's acid ...[more]

PMID: 26663984

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