Reaction reveals direct construction of a [7-5-7-6] tetracyclic framework, suggesting new synthetic routes.
Herein, we report an efficient approach for the direct synthesis of the [7-5-7-6] tetracyclic framework of daphnipaxinin, which contains two synthetically challenging medium-sized rings. The acid-promoted type I [5 + 2] cycloaddition reaction was used as the key step, which directly constructed a synthetically challenging [7-7] fused A/D ring system and the desired all-carbon quaternary stereocenter diastereoselectively.
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Min et al. (2025) studied this question.
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