748164-68-3Relevant academic research and scientific papers
Conversion of 3-arylphthalides into anthrones with a methylcarbonyl substituent at the C-10 position
Bieniek, Adam,Bartczak, Monika M.,Epsztajn, Jan
scheme or table, p. 151 - 153 (2009/10/15)
The ortho-lithiation of a benzoic acid anilide followed by condensation with an aryl aldehyde gave a 3-arylphthalide. Reductive alkylation with 1-methoxy-1-trimethylsilyloxyethene gave a substituted aromatic carboxylic acid which was cyclised to an anthro
Application of organolithium and related reagents in synthesis, part 31: Effective conversion of 3-arylphthalides into 2-(1-aryl-3-oxo-4- alkoxycarbonylbutyl) benzoic acids
Bieniek, Adam,Kulikiewicz, Krystyna K.,Bartczak, Monika M.
, p. 3249 - 3259 (2007/10/03)
A convenient three-step protocol preparation of the ortho-alkylated (longchain substituent with terminal methylcarbonyl or acetoacetate moiety) aromatic carboxylic acids 15 or 16 from benzoic acids anilides 10 was developed, which exploited the reductive
