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Isolation and Ionization of 1,1-Dihalogeno-1H-cyclopropa [a]-naphthalene

Published inChimia, vol. 39, no. 11, p. 362-363
Publication date1985-11
Abstract

1,1-Difluoro- and 1,1-dichloro-1H-cyclopropa[a]naphtbalenes (1a and 1b) are prepared via dehydrohalogenation of the appropriate brominated carbene adducts (2a and 2b, respectively) of 4-bromo-1,2-dihydronaphthalene. Upon dissolution of 1a in cold fluorosulfonic acid it furnishes the very short-lived cation 3; the latter is characterized by its 1H- and 19F-NMR spectra.

Citation (ISO format)
MULLER, Paul, GODOY-NGUYEN THI, Huong Can. Isolation and Ionization of 1,1-Dihalogeno-1H-cyclopropa [a]-naphthalene. In: Chimia, 1985, vol. 39, n° 11, p. 362–363.
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  • PID : unige:167580
Journal ISSN0009-4293
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