| Literature DB >> 23656490 |
Sayuri Yamaguchi1, Tsukasa Hirokane, Takashi Yoshida, Takashi Tanaka, Tsutomu Hatano, Hideyuki Ito, Gen-ichiro Nonaka, Hidetoshi Yamada.
Abstract
Prompted by the outcome that the synthesized roxbin B was not identical to the natural roxbin B, the structural determination process and spectral data were re-examined, with the finding that roxbin B was very likely to be 1-O-galloyl-2,3-(R);4,6-(S)-bis-O-hexahydroxydiphenoyl-β-d-glucose (cuspinin). Because the (R)-axial chirality is rare in natural products when the hexahydroxydiphenoyl group bridges the 2- and 3-oxygens, the proposed structure of cuspinin was confirmed by the total synthesis, leading to the conclusion that roxbin B is the same as cuspinin.Entities:
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Year: 2013 PMID: 23656490 DOI: 10.1021/jo400562k
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354