81739-27-7Relevant articles and documents
Total Synthesis of Casuarinin
Wakamori, Shinnosuke,Matsumoto, Shintaro,Kusuki, Reina,Ikeuchi, Kazutada,Yamada, Hidetoshi
supporting information, p. 3392 - 3396 (2020/05/22)
This study involves the total synthesis of casuarinin, a naturally occurring ellagitannin, in which an open-chain glucose is esterified with two (S)-hexahydroxydiphenoyl (HHDP) groups. One HHDP group incorporates a C-glycosidic bond between its benzene ring and the glucose moiety, which was constructed with complete stereoselectivity using a benzyl oxime group that opened the glucopyranose ring and acted as a scaffold for C-glycoside production. This total synthesis enables future structure-activity relationship studies of this compound.
Casuariin, stachyurin and strictinin, new ellagitannins from Casuarina stricta and Stachyurus praecox
Okuda,Yoshida,Ashida,Yazaki
, p. 766 - 769 (2007/10/02)
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