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A method for introducing a carboxyl substituent into aromatic compounds

โœ Scribed by M. Derenberg; P. Hodge


Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
192 KB
Volume
12
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


When treated with the butoxide-water reagent many benzophenones are cleave to give high yields of benzoic acids.


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Trifluoromethyi derivatives of aromatic molecules were prepared from aromatic halides, converted to dithiocarboxylic acids through formation of Grigmrd reagents, followed by fluorination with xenon diiluoridc at room temperature. The physicochemical properties and biological activities of various ar