Synthesis of the furo[2,3-b]chromene ring system of hyperaspindols a and B

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Abstract

The synthesis of the unique furo[2,3-b]chromene ring system found in hyperaspidinols A and B, acylphloroglucinols from Hypericum chinense has been achieved in twelve steps. By comparison of the NMR spectra of the synthesized compounds with those of the natural products, a relative stereochemistry is suggested, especially that of the ketal carbon.

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Paterson, D. L., & Barker, D. (2015). Synthesis of the furo[2,3-b]chromene ring system of hyperaspindols a and B. Beilstein Journal of Organic Chemistry, 11, 265–270. https://doi.org/10.3762/bjoc.11.29

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