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Merck
CN

Total synthesis of (-)-corilagin.

Journal of the American Chemical Society (2008-05-29)
Hidetoshi Yamada, Kohei Nagao, Kazutoyo Dokei, Yusuke Kasai, Naoki Michihata
摘要

The synthesis of corilagin was achieved by the integration of the development of the oxidative coupling of the symmetrically protected gallates and the temporarily ring-opened synthetic route for the 3,6-hexahydroxydiphenoyl (HHDP) bridge. This is the first total synthesis of the 1C4/B-ellagitannins, which contain ring-flipped glucose.

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Sigma-Aldrich
Corilagin
Supelco
Corilagin, analytical standard