Issue 15, 1983

Catalysis and regioselectivity of quinone Diels–Alder reactions

Abstract

In a series of six different cycloadditions of unsymmetrical quinones and alkyl-substituted butadienes, TiCl4 afforded considerable catalysis (–78 °C) and gave regioselectivity identical with that of the thermal reaction (200 °C) and therefore complementary to that BF3 catalysis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 837-838

Catalysis and regioselectivity of quinone Diels–Alder reactions

J. B. Hendrickson and V. Singh, J. Chem. Soc., Chem. Commun., 1983, 837 DOI: 10.1039/C39830000837

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