Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5166417 | Phytochemistry | 2009 | 9 Pages |
Abstract
The natural α-bisabolol β-d-fucopyranoside (5b) as well as five analogues were efficiently synthesized in excellent yields (83-85%) using Schmidt's inverse procedure. α-Bisabolol α-l-rhamnopyranoside (6b) exhibited the strongest cytotoxic activity against cancer cell lines (IC50 40-64 μM).
Related Topics
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Authors
Marianne Piochon, Jean Legault, Charles Gauthier, André Pichette,