Facile Synthesis of Acacetin-7-O-β-d-Galactopyranoside

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dc.contributor.authorZacharia, James T.
dc.contributor.authorHayashi, Masahiko
dc.date.accessioned2016-09-21T13:42:14Z
dc.date.available2016-09-21T13:42:14Z
dc.date.issued2011-12
dc.descriptionFull text can be accessed at http://www.sciencedirect.com/science/article/pii/S0008621511005714en_US
dc.description.abstractAcacetin-7-O-β-d-galactopyranoside (1), a natural flavonoid isolated from flower heads of Chrysanthemum morifolium, has been reported to inhibit the replication of HIV in H9 cells. We achieved the total synthesis of compound 1 by employing a one-pot synthesis of the aglycon. The key reactions in this approach include the modified Baker–Venkataraman reaction and regio- and stereoselective O-glycosylations.en_US
dc.identifier.citationZacharia, J.T. and Hayashi, M., 2012. Facile synthesis of acacetin-7-O-β-D-galactopyranoside. Carbohydrate research, 348, pp.91-94.en_US
dc.identifier.doi10.1016/j.carres.2011.11.015
dc.identifier.urihttp://hdl.handle.net/20.500.11810/3977
dc.language.isoenen_US
dc.titleFacile Synthesis of Acacetin-7-O-β-d-Galactopyranosideen_US
dc.typeJournal Articleen_US
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