Title of article :
Facile synthesis of acacetin-7-O-β-d-galactopyranoside
Author/Authors :
James T. Zacharia، نويسنده , , Masahiko Hayashi، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2012
Abstract :
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.
Keywords :
Flavonoid , Aglycon , Glycosyl fluoride , Acacetin-7-O-?-d-galactopyranoside , O-Glycosylation
Journal title :
Carbohydrate Research
Journal title :
Carbohydrate Research