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
Pages
4
From page
91
To page
94
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
Serial Year
2012
Journal title
Carbohydrate Research
Record number
967454
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