Abstract

A new synthesis of O-methyldauricine has been effected through an intermediate bisthioamide obtained by means of the Wilgerodt-Kindler reaction from 2-acetyl-5-methoxyphenyl 4′-acetylphenyl ether and homoveratrylamine. Subsequent Bischler-Napieralski cyclization, methylation, and reduction yielded racemic O-methyldauricine.

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