The substitution of primary or secondary alcohols with nucleophiles mediated by a redox
combination of a trialkylor triarylphosphine and a dialkyl azodicarboxylate is popularly …

While natural and synthetic N-nucleosides are vulnerable to enzymatic and acid-catalyzed
hydrolysis of the nucleosidic bond, their C-analogues are much more stable. Several C …

An efficient and general approach for the synthesis of indolyl-C-glycosides via
aminopalladation and subsequent Heck-type glycosylation of easily available 2 …

We described a novel palladium-catalyzed C–H glycosylation of indole or tryptophan for a
one-pot stereoselective synthesis of 2, 3-diglycosylindoles and tryptophan-C-glycosides. In …

We describe the palladium-catalyzed direct C–H glycosylation of free NH indole or
tryptophan for the stereoselective synthesis of 2-glycosylindoles and tryptophan-C …

The study and synthesis of C-nucleosides has been extensive owing to their biological
activity and potential as drug candidates for antiviral and anticancer therapy. Numerous …

The alkene-based o-[1-(p-MeO-phenyl) vinyl] benzoates (PMPVB) donors that can be
remotely activated under catalytic Brønsted acidic conditions have been utilized to …

A five-step practical and stereocontrolled synthesis of α-and β-pseudouridines from d-
ribonolactone is described. The key step involves a highly stereoselective reduction of a …

An efficient and highly regioselective method for the synthesis of 3-indolyl-C-glycosides has
been developed through coupling of glycosyl trichloroacetimidates with a wide range of …

Total Synthesis of (−)‐Isatisine A × Close The Infona portal uses cookies, ie strings of text
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