Issue 11, 1971

Direct observation of conjugated bis-ketene and ketene–ketenimine intermediates in the photolysis of diphenylcyclobutenedione derivatives

Abstract

The photolysis of diphenylcyclobutenedion (Ia) and its imine derivative (Ib) in the presence of an isonitrile gives ring-expanded products (IIIa) and (IIIb)via conjugated bis-ketene (IIa) and ketene-ketenimine (IIb) intermediates, which were confirmed by the photolysis of (I) in methanol to give succinate (IV) and directyl by i.r. spectroscopy during low temperature photolysis.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 587-588

Direct observation of conjugated bis-ketene and ketene–ketenimine intermediates in the photolysis of diphenylcyclobutenedione derivatives

N. Obata and T. Takizawa, J. Chem. Soc. D, 1971, 587 DOI: 10.1039/C29710000587

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