Facile Synthesis of Acacetin-7-O-β-d-Galactopyranoside
| dc.creator | Zacharia, James T. | |
| dc.creator | Hayashi, Masahiko | |
| dc.date | 2016-09-21T13:42:14Z | |
| dc.date | 2016-09-21T13:42:14Z | |
| dc.date | 2011-12 | |
| dc.date.accessioned | 2018-03-27T08:55:01Z | |
| dc.date.available | 2018-03-27T08:55:01Z | |
| dc.description | Full text can be accessed at http://www.sciencedirect.com/science/article/pii/S0008621511005714 | |
| dc.description | Acacetin-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. | |
| dc.identifier | Zacharia, J.T. and Hayashi, M., 2012. Facile synthesis of acacetin-7-O-β-D-galactopyranoside. Carbohydrate research, 348, pp.91-94. | |
| dc.identifier | http://hdl.handle.net/20.500.11810/3977 | |
| dc.identifier | 10.1016/j.carres.2011.11.015 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11810/3977 | |
| dc.language | en | |
| dc.title | Facile Synthesis of Acacetin-7-O-β-d-Galactopyranoside | |
| dc.type | Journal Article |