Zacharia, James T.Hayashi, Masahiko2016-09-212016-09-212011-12Zacharia, J.T. and Hayashi, M., 2012. Facile synthesis of acacetin-7-O-β-D-galactopyranoside. Carbohydrate research, 348, pp.91-94.http://hdl.handle.net/20.500.11810/3977Full text can be accessed at http://www.sciencedirect.com/science/article/pii/S0008621511005714Acacetin-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.enFacile Synthesis of Acacetin-7-O-β-d-GalactopyranosideJournal Article10.1016/j.carres.2011.11.015