Structural establishment of polygalatenosides A and B by total synthesis

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Abstract

The first total synthesis of polygalatenosides A (1) and B (2), originally isolated from the traditional Chinese medicine and reported as antidepressant agents, is described here. Glycosylation between thiogalactosyl donors 6 and 7 and 1-deoxyglucosyl acceptor 5 yielded the corresponding key intermediates 10 and 16, respectively, with an α(1→2)-glycosidic linkage in moderate yields. In addition, d-configuration of the galactoside residue in 1 and 2 was confirmed in our studies. © 2008 Elsevier Ltd. All rights reserved.

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Huang, C. M., Liu, R. S., Wu, T. S., & Cheng, W. C. (2008). Structural establishment of polygalatenosides A and B by total synthesis. Tetrahedron Letters, 49(18), 2895–2898. https://doi.org/10.1016/j.tetlet.2008.03.032

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