Issue 10, 1989

Synthesis and some reactions of 3,3,6-trisubstituted tricyclo[3.2.0.01,4]heptan-2-ones

Abstract

Electrophiles and most nucleophiles react with tricyclo[3.2.0.01,4]heptan-2-ones with preferential cleavage of the C(1)–C(4) or C(1)-C(5) bond; X-ray data show the highly strained tricycloheptanone (14) has a bond angle of 149.2(9)° at a tetravalent carbon atom.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 670-672

Synthesis and some reactions of 3,3,6-trisubstituted tricyclo[3.2.0.01,4]heptan-2-ones

H. Finch, R. M. Highcock, S. M. Roberts, K. M. Short and V. Sik, J. Chem. Soc., Chem. Commun., 1989, 670 DOI: 10.1039/C39890000670

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