Reinvestigation of absolute stereostructure of (-)-rosiridol: Structures of monoterpene glycosides, rosiridin, rosiridosides A, B, and C, from Rhodiola sachalinensis

23Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

Three new (-)-rosiridol glycosides, rosiridosides A, B, and C, were isolated from the roots of Rhodiola sachalinensis together with rosiridin [(-)-rosiridol 1-O-β-D-glucopyranoside]. In the course of the structure elucidation of those new glycosides, the absolute configuration of the 4-position in (-)-rosiridol was reinvestigated. On the basis of the application of the modified Mosher's method for (-)- and (+)-rosiridol derivatives, the absolute configuration of the 4-position in (-)-rosiridol should be revised to be S orientation from the recently assigned R form, so that the absolute stereostructures of rosiridosides A, B, and C and rosiridin were determined. © 2008 Pharmaceutical Society of Japan.

Cite

CITATION STYLE

APA

Yoshikawa, M., Nakamura, S., Li, X., & Matsuda, H. (2008). Reinvestigation of absolute stereostructure of (-)-rosiridol: Structures of monoterpene glycosides, rosiridin, rosiridosides A, B, and C, from Rhodiola sachalinensis. Chemical and Pharmaceutical Bulletin, 56(5), 695–700. https://doi.org/10.1248/cpb.56.695

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free