Synthesis of dienes from pyrrolidines using skeletal modification

Abstract

Saturated N-heterocyclic pyrrolidines are common in natural products, medicinal compounds and agrochemicals. However, reconstruction of their skeletal structures creating new chemical space is a challenging task, and limited methods exist for this purpose. In this study, we report a skeletal modification strategy for conversion of polar cyclic pyrrolidines into nonpolar linear dienes through a N-atom removal and deconstruction process. This involves N-sulfonylazidonation followed by rearrangement of the resulting sulfamoyl azide intermediates. This can be an energetically unfavorable process, which involves the formation of active C–C π bonds, the consumption of inert C–N and C–C σ bonds and the destruction of stable five-membered rings, but we have used it here to produce versatile conjugated and nonconjugated dienes with links of varying lengths. We also studied the application of this method in late-stage skeletal modification of bioactive compounds, formal traceless C(sp2)–H functionalization and formal N-atom deletion.

Description
© 2023, The Author(s). cc-by
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Citation
Qin, H., Guo, T., Lin, K., Li, G., & Lu, H.. 2023. Synthesis of dienes from pyrrolidines using skeletal modification. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-43238-7
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