6587-77-5

Upstream product

• 108-24-7 acetic anhydride 
• 29971-56-0 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol 
• 5517-47-5 1⁽³⁾,2,4⁽⁶⁾,5,6⁽⁴⁾-penta-O-acetyl-sn-myo-inositol 
• 28140-37-6 3,4,6-tri-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-D-mannopyranoside 
• 2347-99-1 1-O-α-D-mannopyranosyl-sn-myo-inositol 
• 210281-95-1 β-D-mannopyranosyl fluoride 
• 4715-05-3 3,4,6-tri-O-acetyl-α-D-glucopyranose-1,2-(t-butylorthoacetat) 
• 29971-56-0 1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol 

Downstream Products

• 35519-39-2 1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myoinositol 
• 6605-49-8 α-D-mannopyranosyl-sn-myo-inositol 
• 2347-99-1 1-O-α-D-mannopyranosyl-sn-myo-inositol 

Relevant academic research and scientific papers

Creation of an α-mannosynthase from a broad glycosidase scaffold

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

INVESTIGATIONS IN THE REGION OF ASYMMETRICALLY SUBSTITUTED MYO-INOSITOL DERIVATIVES XXXIV. SYNTHESIS OF DIASTEREOMERIC ACETATES OF β-D-GLUCOSYL-MYO-INOSITOL AND CHIRAL MYO-INOSITOL PENTAACETATES

The glucosylation of racemic tetra- and pentaacetyl-myo-inositols by D-glucose tert-butylorthoacetate leads to a mixture of diastereomeric acetate derivatives of β-D-glucosyl-myo-inositol.Chiral pentaacetyl-myo-inositols were obtained from the synthesized

DERIVATIVES OF ASYMMETRICALLY SUBSTITUTED MYO-INOSITOL. XXXIII. SYNTHESIS OF DIASTEROMERIC MANNOSIDES OF MYO-INOSITOL

Diastereomeric acetylated mannosides of myo-inositol were synthesized by the glycosylation of the racemic acetates of myo-inositol with the ethyl orthoacetate of D-mannose.The synthesized mannosides of myo-inositol can be used for the production of chiral myo-inositol acetates and as intermediates in the synthesis of complex phosphoinositides.