Saturated oxygen heterocycles - Journal of the Chemical Society, Perkin Transactions 1 (RSC
Publishing) DOI:10.1039/B201515N Royal Society of Chemistry View PDF VersionNext …

After the development of accelerators as neutron source, the access to new suitable agents
for boron neutron capture therapy (BNCT) became a major need. Among many others, sugar …

The key THF derivative (9a) for an enantioselective synthesis of amphidinolide X/Y was
obtained from 1a via a selenoetherification reaction. In fact, among the cyclization methods …

A general procedure for the stereoselective synthesis of 2-deoxy-2-iodo-hexo-and-hepto-
pyranosyl glycosides from furanoses is reported. The proposed methodology provides a …

Diphenyldisulfone is a mild and efficient reagent for selective cleavage of methylprenyl (2, 3-
dimethylbut-2-en-1-yl), prenyl (3-methylbut-2-en1-yl), and methallyl (2-methylallyl) ethers …

A high yielding and convenient synthesis of 2-aryl-2, 5-dihydro-2H-pyrans is reported.
Sonogashira coupling of 4-pentyn-1-ol and 5-hexyn-2-ol with a range of phenyl and …

The work described herein considers the impact of stereoelectronic effects and allylic 1, 3-
strain in controlling the cyclofunctionalization reaction when a hydroxyl group is at the allylic …

Abstract A series of 2‐deoxy‐2‐phenylselenenyl‐1‐thioglycosides were evaluated as a
class of glycosyl donors that provide access to 2‐deoxyglycosides from furanoses. This short …

Novel type of Pd (II)-catalysed transformation of sugar-derived alkenitols furnishing 7-
benzyloxy-2, 5-dioxabicyclo [2.2. 1] heptanes was discovered. The investigated bicyclisation …

A new and highly efficient methodology for the stereocontrolled synthesis of
aminodeoxyalditols is described through a dimesylation/intramolecular SN 2 nucleophilic …