149656-37-1

Upstream product

• 27851-29-2 benzyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 23262-92-2 (+/-)-1-O-benzoyl-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 26276-99-3 rac-1,4,5,6-tetra-O-benzyl-myo-inositol 
• 183953-29-9 benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 39687-26-8 (2R,3R,4S,5S,6S)-2,3,4,5-Tetrakis-benzyloxy-6-iodomethyl-tetrahydro-pyran 
• 638203-33-5 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol 
• 638203-45-9 C₄₄H₅₀O₆ 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 177471-67-9 3,4,5,6-tetra-O-benzyl-2-deoxy-scyllo-inosose 
• 189222-32-0 (2R,3R,4S,5S)-2,3,4,5-Tetrakis-benzyloxy-6-methylene-tetrahydro-pyran 

Relevant academic research and scientific papers

L-chiro-inositol derivatives from myo-inositol. Building blocks for inositolphosphoglycans

A straightforward synthesis of L-chiro-inositol, deoxy L-chiro-inositol derivatives and L-chiro-inositol building blocks for the preparation of inositolphosphoglycans, is reported from myoinositol. Glycosylation with 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-g

Novel carbocyclic ring closure of hex-5-enopyranosides

Retention of configuration at the anomeric carbon atom is observed for a novel rearrangement of carbohydrates. The readily accessible vinyl acetal 1 undergoes a triisobutylaluminum-assisted, stereoselective transposition of an oxygen atom on the ring with

Synthesis of 2- and 6-Deoxyinostol 1-Phosphate and the Role of the Adjecent Hydroxy Groups in the Mechanism of Inositol Monophosphatase

The 2- and 6-hydroxy groups of myo-inositol 1-phosphate have been shown to be independently associated with the mechanisms of hydrolysis and binding in the dephosporylation of the substrate by inositol monophosphatase.