Abstract
AbstractDescribed is a formal synthesis of racemic schulzeines B and C that intercepts intermediates developed by Gurjar and co‐workers. The synthetic sequence features an annulative coupling of a ketimine and acrylic acid enabling the construction of the benzoquinolizidine nucleus in a highly convergent manner. We also examined a continuous‐flow version of the thermal aza‐annulation, which proved less practical as compared to the batch processes.
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