1910
DOI: 10.1039/ct9109701960
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CCVIII.—The formation of tolane derivatives from p-chlorotoluene and 3 : 4-dichlorotoluene

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1938
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Cited by 14 publications
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“…After two recrystallizations of this mixture using acetone, the cis isomer was isolated [mp 167-168.5 °C; lit. mp 166-167 °C (Kenner and Witham, 1910;Fleck, 1948)].…”
Section: Methodsmentioning
confidence: 99%
“…After two recrystallizations of this mixture using acetone, the cis isomer was isolated [mp 167-168.5 °C; lit. mp 166-167 °C (Kenner and Witham, 1910;Fleck, 1948)].…”
Section: Methodsmentioning
confidence: 99%
“…4,4'-Dimethyldiphenylacetylene (9) and 4,4'-dimethoxydiphenylacetylene (13) were prepared by mercuric oxide oxidation of their respective benzil bishydrazones (1,5,13). 4,4'-Bis(dimethylamino)diphenylacetylene (7) and 4,4'-dichlorodiphenylacetylene (6,9) were prepared by reaction of their respective benzils (8, 14, 15) with triethyl phosphite (9). 4,4'-Dinitrodiphenylacetylene (12) was prepared by dehydrohalogenation of 4,4'-dinitrostilbene dibromide (12).…”
Section: Methodsmentioning
confidence: 99%