Synthesis of C-Aryl Furanosides by the “Reverse Polarity” Strategy
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (6) , 2191-2194
- https://doi.org/10.1021/jo951344o
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Reductive and Nonreductive Aromatization of Quinol Ketal Glycals. Models for the Preparation of C-Aryl Glycoside Natural ProductsThe Journal of Organic Chemistry, 1995
- Methodology for the Regiospecific Synthesis of Bis C-Aryl Glycosides. Models for KidamycinsJournal of the American Chemical Society, 1994
- Reductive aromatization of quinols. New convenient methods for the regiospecific synthesis of p-hydroxy C-aryl glycalsThe Journal of Organic Chemistry, 1992
- An efficient synthesis of hydroxyethylene dipeptide isosteres: the core unit of potent HIV-1 protease inhibitorsThe Journal of Organic Chemistry, 1991
- Reductive aromatization of quinol ketals: a new synthesis of C-aryl glycosidesJournal of the American Chemical Society, 1991
- A new method for synthesis of trifluoromethyl-substituted phenols and anilinesThe Journal of Organic Chemistry, 1989
- Convergent synthesis of polyether ionophore antibiotics: an approach to the synthesis of the monensin tetrahydropyran-bis(tetrahydrofuran) via the ester enolate Claisen rearrangement and reductive decarboxylationJournal of the American Chemical Society, 1985
- Mechanism of the oxidation of NADH by quinones. Energetics of one-electron and hydride routesJournal of the American Chemical Society, 1985
- Enolate Claisen rearrangement of esters from furanoid and pyranoid glycalsThe Journal of Organic Chemistry, 1980
- Anodic oxidation as a synthetic expedient to naphthoquinone mono- and bisketalsTetrahedron Letters, 1977