Abstract: Isoselagintamarlin A (1), a selaginellin analogue featured a rare benzofuran unit, was isolated from Selaginella tamariscina. Its complete structural assignment was established through a combination of high-field NMR technique and biomimetic synthesis. Notably, isoselagintamarlin A (1) was successfully synthesized via sequential oxidations and intramolecular cyclization. Graphical Abstract: [Figure not available: see fulltext.].
CITATION STYLE
Zhu, Q. F., Shao, L. D., Wu, X. D., Liu, J. X., & Zhao, Q. S. (2019). Isolation, Structural Assignment of Isoselagintamarlin A from Selaginella tamariscina and Its Biomimetic Synthesis. Natural Products and Bioprospecting, 9(1), 69–74. https://doi.org/10.1007/s13659-018-0195-5
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