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Stereochemistry of the Diels-Alder Addition of Halogenated Cyclopropenes

Published inChimia, vol. 41, p. 244-245
Publication date1987
Abstract

The structures of two cycloadducts (1 and 2) of cyclopropenes to 1 ,3-diphenylisobenzofuran and trans-1-phenylbutadiene are established by X-ray crystallography. Both are exo adducts. In 2 the phenyl substituent occupies a pseudo-axial position; the ring-flipped conformation (2a) with the phenyl ring pseudo-equatorial is not observed.

Citation (ISO format)
MULLER, Paul et al. Stereochemistry of the Diels-Alder Addition of Halogenated Cyclopropenes. In: Chimia, 1987, vol. 41, p. 244–245.
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  • PID : unige:167155
Journal ISSN0009-4293
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