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DOI: 10.1039/A900282K (Paper) Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1999, 1353-1358

Structure and stereochemistry of cyclodimers obtained by acid treatment of trans-stilbenes and of N-1,2-diarylethylamides

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José M. Aguirre, Elba N. Alesso and Graciela Y. Moltrasio Iglesias

Abstract

The reaction of trans-stilbenes and N-1,2-diarylethylamides with ethyl polyphosphate affords indanes and tetralins with three stereogenic centres. The structural and configurational assignment of the cyclodimers is based mainly on the NMR and MS data. A possible transition state for the reaction is discussed.

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