112239-09-5Relevant academic research and scientific papers
THE SYNTHESIS OF 9-OXO-9,10-DIHYDROACRIDINE-4-CARBOXYLIC ACIDS VIA THE JOURDAN-ULLMANN REACTION OF ANTHRANILIC ACIDS AND METHYL 2-IODOBENZOATES
Rewcastle, Gordon W.,Denny, William A
, p. 309 - 318 (2007/10/02)
Reaction between anthranilic acids and methyl 2-iodobenzoates under anhydrous Jourdan-Ullmann conditions gives good to excellent yields of 2-(2-methoxycarbonylphenyl)anthranilic acids, required precursors for the unequivocal synthesis of substituted 9-oxo
Potential Antitumor Agents. 46. Structure-Activity Relationships for Acridine Monosubstituted Derivatives of the Antitumor Agent N--9-aminoacridine-4-carboxamide
Rewcastle, Gordon W.,Atwell, Graham J.,Chambers, David,Baguley, Bruce C.,Denny, William A.
, p. 472 - 477 (2007/10/02)
A series of monosubstituted derivatives of the new antitumor agent N--9-aminoacridine-4-carboxamide has been prepared, bearing methyl, methoxy, and chloro groups at available acridine positions.The physicochemical properties and an
