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학술저널

7,8-Dioxo-A-norerythrinan의 합성

Synthesis of 7,8-Dioxo-A-norerythrinan

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7,8-Dioxo-A-norerythrinan (A) was synthesized from acid catalyzed cyclization of 6a-hydroxy-1-(2-phenylethyl)-octahydrocyclo-penta[b]pyrrole-3a-carboxylic acid ethyl ester (B) with concomitant deethoxycarbonylation. The intermediate (B) was a hydroxylated compound of N-acyliminium (C). The unstable pyrrolinium (C) was prepared from oxalylation of the enamine of phenethylamine and ethyl 2-oxocyclopentanecarboxylate.

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