288307-76-6

Upstream product

• 530-26-7 D-Mannose 
• 62-53-3 aniline 
• 7322-31-8 β-D-mannose 
• 3458-28-4 D-Mannose 

Downstream Products

• 151767-38-3 tetra-O-acetyl-N-phenyl-β-D-mannopyranosylamine 

Relevant academic research and scientific papers

Synthesis of bis(glycosylamino)alkanes and bis(glycosylamino)arenes

The condensation of D-mannose and D-galactose with aliphatic and aromatic diamines afforded a series of bis(glycosylamino)alkanes and-arenes. A possible mechanism was proposed for the formation of 1,2-bis(β-D-glycosylamino) benzenes.

Schiff bases or glycosylamines: Crystal and molecular structures of four derivatives of D-mannose

Crystal and molecular structures of four derivatives of D-mannose are described. Each could exist as either an open-chain Schiff base or as a glycosylamine in the solid state. The derivative formed upon reaction of D-mannose with hydroxylamine is an open-chain oxime, but those formed upon reaction with semicarbazide, aniline, and p-chloroaniline are glycosylamines. The oxime, which crystallizes as the syn-(E) isomer, has a fully extended carbon chain. The glycosylamines are all β-pyranoses. The packing arrangement of the oxime involves 'head-to-tail' hydrogen bonding. The semicarbazide derivative, which crystallizes as a dihydrate, features a hydrogen-bonded intramolecular bridge formed by the two water molecules and linking O-6 to the carbonyl oxygen atom. The packing arrangements of the aniline and p-chloroaniline derivatives differ from each other but are nevertheless closely related by similar hydrogen-bonding interactions. Copyright (C) 2000 Elsevier Science Ltd.

Synthesis and antiproliferative activity of selenoindirubins and selenoindirubin-N-glycosides

Selenoindirubins and selenoindirubin-N-glycosides were prepared by the reaction of isatins and isatin-N-glycosides with 3-acetoxy-benzo[b]selenophene, respectively. While selenoindirubin-N-glycosides have not been reported before, three non-glycosylated s