| 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.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.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.language |
en |
|
| dc.title |
Facile Synthesis of Acacetin-7-O-β-d-Galactopyranoside |
|
| dc.type |
Journal Article |
|