Issue 7, 1980

The hydrogen-bond as a configurational lock in the photocyclisation of dibenzoylmethane o-halogenoanils: wavelength dependence of this reaction

Abstract

The tautomers (1, X[double bond, length as m-dash]Cl, Br, or I) of anils photocyclise to the phenanthridine derivative (2) with varying efficiencies depending on the halogen and the solvent; owing to the low energies of the first excited states the quantum yields vary with irradiation wavelength.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 301-302

The hydrogen-bond as a configurational lock in the photocyclisation of dibenzoylmethane o-halogenoanils: wavelength dependence of this reaction

J. Grimshaw and A. P. de Silva, J. Chem. Soc., Chem. Commun., 1980, 301 DOI: 10.1039/C39800000301

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