Issue 0, 1971

The synthesis and ultraviolet and nuclear magnetic resonance spectra of some 9-substituted 9,10-dihydroacridines

Abstract

The n.m.r. spectra of a series of 9-substituted 9,10-dihydroacridines are consistent with a molecular conformation in which a central boat-shaped ring has the larger substituent in the pseudo-axial orientation. The u.v. spectra of 9,10-dihydro-9-t-butylacridine and its derivatives show absorption maxima absent from the spectra of other 9,10-dihydroacridines.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 2537-2538

The synthesis and ultraviolet and nuclear magnetic resonance spectra of some 9-substituted 9,10-dihydroacridines

G. A. Taylor and S. A. Procter, J. Chem. Soc. C, 1971, 2537 DOI: 10.1039/J39710002537

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