| Literature DB >> 11674105 |
Ken S. Feldman1, Kiran Sahasrabudhe.
Abstract
The first chemical synthesis of the naturally occurring ellagitannin tellimagrandin II is reported. Key steps of the synthesis include the atropselective oxidative coupling of suitably protected galloyl rings at the O(4) and O(6) positions of a glucopyranose core, and the stereoselective acylation of the derived anomeric alcohol with a galloyl chloride. In addition, the synthesis of a novel gallotannin-ellagitannin hybrid is described. This dimeric construct relied on a hetero Diels-Alder cycloaddition/reductive rearrangement sequence to deliver the intact skeleton from a monomeric pentagalloylglucose-based orthoquinone.Entities:
Year: 1999 PMID: 11674105 DOI: 10.1021/jo9816966
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354