75316-81-3

Upstream product

• 75316-80-2 1,6-anhydro-4-O-benzyl-3-O-(N-benzylcarbamoyl)-2-O-p-tolylsulfonyl-β-D-glucopyranose 
• 20183-65-7 1,6-anhydro-4-O-benzyl-2-O-(4-toluenesulfonyl)-β-D-glucopyranose 
• 3173-56-6 benzyl isothiocyanate 

Downstream Products

• 75316-82-4 3-benzyl-(1,6-anhydro-2,3-dideoxy-β-D-mannopyrano)<2,3-d>oxazolidin-2-one 
• 75316-84-6 1,6-anhydro-4-O-benzyl-2-benzylamino-2-deoxy-β-D-mannopyranose 

Relevant academic research and scientific papers

PREPARATION OF 2-AMINO-1,6-ANHYDRO-2,3-DIDEOXY-β-D-arabino-HEXOPYRANOSE. 1H- AND 13C-N. M. R. SPECTRA OF DEOXY DERIVATIVES OF 2-AMINO-1,6-ANHYDRO-2-DEOXY-D-GLUCOSE AND 2-AMINO-1,6-ANHYDRO-2-DEOXY-D-MANNOSE

Partial benzyloxycarbonylation of 1,6-anhydro-D-mannosamine, subsequent mesylation, and treatment with sodium methoxide gave 1,6:3,4-dianhydro-2-benzyloxycarbonylamino-2-deoxy-β-D-altropyranose (9).Oxirane-ring cleavage in 9 with potassium iodide, acetyla

PREPARATION OF 2-AMINO-1,6-ANHYDRO-2-DEOXY-β-D-MANNOPYRANOSE BY INTRAMOLECULAR SUBSTITUTION OF THE TOSYLOXY GROUP IN STERICALLY HINDERED POSITION OF 1,6-ANHYDRO-2-O-p-TOLYLSULFONYL-β-D-GLUCOPYRANOSE

1,6:3,4-Dianhydro-2-O-p-tolylsulfonyl-β-D-galactopyranose (I) was converted to 1,6-anhydro-4-O-benzyl-2-O-p-tolylsulfonyl-β-D-glucopyranose (II) and then reacted with benzylisocyanate to give 3-O-(N-benzylcarbamoyl) derivative III.The cyclization of this