Collective Total Synthesis of Aculeatin A, B, D, E, and F
Manoj Kumar1, Parthasarathi Subramanian1
1Department of Chemistry, Indian Institute of Technology, Kanpur, Uttar Pradesh 208016, India.
The Journal of Organic Chemistry
|February 5, 2025
Abstract:
A collective convergent approach for the enantioselective total synthesis of aculeatins A, B, D, E, and F is presented, featuring [3 + 2]-cycloaddition, iron-mediated reductive N-O bond cleavage, and cascade spirocyclization. Moreover, this short six-step strategy is supplemented in synthesizing unnatural analogs of aculeatins such as 6-epi-aculeatin D, 6-epi-aculeatin E, and 6-epi-aculeatin F.
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