CHEMICAL STUDIES ON CRUDE DRUG PROCESSING .9. ON THE CONSTITUENTS OF REHMANNIAE RADIX .3. ABSOLUTE STEREOSTRUCTURES OF REHMAIONOSIDE-A, REHMAIONOSIDE-B, AND REHMAIONOSIDE-C, AND REHMAPICROSIDE, BIOLOGICALLY-ACTIVE IONONE GLUCOSIDES AND A MONOTERPENE GLUCOSIDE ISOLATED FROM CHINESE REHMANNIAE RADIX
M. Yoshikawa et al., CHEMICAL STUDIES ON CRUDE DRUG PROCESSING .9. ON THE CONSTITUENTS OF REHMANNIAE RADIX .3. ABSOLUTE STEREOSTRUCTURES OF REHMAIONOSIDE-A, REHMAIONOSIDE-B, AND REHMAIONOSIDE-C, AND REHMAPICROSIDE, BIOLOGICALLY-ACTIVE IONONE GLUCOSIDES AND A MONOTERPENE GLUCOSIDE ISOLATED FROM CHINESE REHMANNIAE RADIX, Chemical and Pharmaceutical Bulletin, 44(1), 1996, pp. 41-47
Following the characterization of the iridoid and iridoid glycoside co
nstituents in Chinese Rehmanniae Radix, the dried root of Rehmannia gl
utinosa LIBOSCH. [Kan-jio in Japanese], we investigated the structures
of biologically active ionone glucosides, rehmaionosides A, B, and C,
and a monoterpene glucoside, rehmapicroside. Their absolute stereostr
uctures were determined on the basis of chemical and physicochemical e
vidence, which included the result of application of the exciton chira
lity method to the allylic benzoyl derivatives.