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Stereoselective synthesises are described for naphthalene and tetralin derivatives. Hexabromo 2 and 3, monomethoxy 7, dimethoxy 6, dihydroxy 4 and dinitroxy 10 derivatives of tetralin have been obtained. Base-promoted elimination reactions of 6 and 4 provided monomethoxy 8 and 9 and diepoxy 5 naphthalenes respectively. The structures of these products were determined by 1 H and 13 C NMR spectra, mass spectra and micro analysis.
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Erenler et al. (2004) studied this question.
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