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Formation of polylithioallenes is a facile process
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Formation of polylithioallenes is a facile process: (a) Jaffe, F. J. Organomet. Chem. 1970, 23, 53.
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2 had been formed by the rearrangement of 1,2-dilithio-3,3-diphenylcyclopropene, the latter having been generated by the dilithiation of 3,3-diphenylcyclopropene by butyllithium
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2 had been formed by the rearrangement of 1,2-dilithio-3,3-diphenylcyclopropene, the latter having been generated by the dilithiation of 3,3-diphenylcyclopropene by butyllithium: Binger, P.; Müller, P.; Wenz, R.; Mynott, R. Angew. Chem., Int. Ed. Engl. 1990, 29, 1037.
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The spectroscopic properties and melting point (194–196 °C) were identical with those of cis-1,2-diphenyl-anti-3,4-dibenzylidenecyclobutane (mp 197 °C), which was prepared by heating 1,3-diphenylallene in refluxing benzene
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The spectroscopic properties and melting point (194–196 °C) were identical with those of cis-1,2-diphenyl-anti-3,4-dibenzylidenecyclobutane (mp 197 °C), which was prepared by heating 1,3-diphenylallene in refluxing benzene: Dehmlow, E. V. Chem. Ber. 1967, 100, 3260.
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