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- W1969708164 abstract "The expedient synthesis of three novel indole analogues, 2a–c, of mycophenolic acid is described, which involved as the key steps both the Et2O·BF3 catalyzed amino-Claisen rearrangement of N-allylindoline to 7-allylindoline and the ortho ester Claisen rearrangement of the allylic alcohol 12 to the methyl ester 14. The installation of the substituents at the C-3 position in 2b and 2c was accomplished via Vilsmeier formylation and subsequent oxidation–aminolysis or oxidation–methoxylation. The synthetic approach described possesses general usefulness. The analogue 2b showed significant, reproducible antitumor activity." @default.
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- W1969708164 title "Synthesis of Novel Indole Analogues of Mycophenolic Acid as Potential Antineoplastic Agents" @default.
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