3, 4, 5‐Trihydroxypiperidines belong to the family of 1, 5‐dideoxy‐1, 5‐iminosugar natural
products and are structural analogues of pentose monosaccharides in the pyranose form …

The reductive amination (RA) reaction plays a pivotal role in the synthesis of new C–N
bonds, due to the availability of many different and low‐cost reagents and their operational …

Considerable interest has been attracted in xanthone and its derivatives because of their
large variety of pharmacological activities. In this project, a series of hydroxylxanthones and …

A series of novel xanthone derivatives with extended π-systems, that is, benzoxanthones 2–
4, and their structurally perturbed analogs 5–9 have been designed and synthesized as α …

Xanthenone based hydrazone derivatives (5a–n) have been synthesized as potential α-
glucosidase inhibitors. All synthesized compounds (5a–n) are characterized by their FTIR …

Synthesis of iminosugars 1, 2, 3a, and 4a and N-alkyl (ethyl, butyl, hexyl, octyl, decyl, and
dodecyl) derivatives 3b–g and 4b–g spiro-linked with morpholine-fused 1, 2, 3-triazole is …

A new general method for the synthesis of a variety of 1-azasugars with a nitrogen atom at
the anomeric position is described. The readily available chiral N-Boc-5-hydroxy-3 …

Hydroxymethylation of α-d-xylo-pentodialdose using excess formaldehyde and sodium
hydroxide in THF–water (one pot aldol and crossed Cannizzaro reactions) followed by …

Gram-negative bacteria have evolved an elaborate process for the recycling of their cell
wall, which is initiated in the periplasmic space by the action of lytic transglycosylases. The …

Synthesis of both enantiomers of pachastrissamine is described from a common chiral
template. The stereoselective construction of the central tetrahydrofuran units was based on …