Issue 19, 1975

Mode of cyclopropane ring opening of 1a,2,3,7b-tetrahydro-1-phenyl-1H-cyclopropa[a]naphthalene: a correction

Abstract

Catalytic hydrogenolysis of 1a,2,3,7b-tetrahydro-1-phenyl-1H-cyclopropa[a]naphthalene (I) and of the corresponding 1a,7b-dihydro-derivative provides 2-benzyltetralin (VI) and not 6,7,8,9-tetrahydro-6-phenyl-5H-benzocycloheptene (II) as previously reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 1934-1936

Mode of cyclopropane ring opening of 1a,2,3,7b-tetrahydro-1-phenyl-1H-cyclopropa[a]naphthalene: a correction

A. Chatterjee, B. Bandyopadhyay and R. Mallik, J. Chem. Soc., Perkin Trans. 1, 1975, 1934 DOI: 10.1039/P19750001934

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