Synthesis of the C-Glycosidic Analogue of Adenophostin A and Its Uracil Congener as Potential IP3 Receptor Ligands. Stereoselective Construction of the C-Glycosidic Structure by a Temporary Silicon-Tethered Radical Coupling Reaction
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0001333
Reference34 articles.
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