637329-52-3

Upstream product

• 638203-45-9 C₄₄H₅₀O₆ 
• 331679-26-6 2,3-O-(D-1,7,7-trimethylbicyclo[2.2.1]hept-6-ylidene)-D-myo-inositol 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 87-89-8 D-myo-inositol 
• 108-24-7 acetic anhydride 
• 638203-33-5 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol 

Downstream Products

• 637329-55-6 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosyl-β-(1->1)-6-O-allyl-2,3,4,5-tetra-O-benzyl-L-chiro-inositol 
• 637329-58-9 (1S,2R,3S,4R,5S,6R)-2-((2S,3R,4R,5S,6R)-3-Azido-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,4,5,6-tetrakis-benzyloxy-cyclohexanol 
• 637329-56-7 Acetic acid (1R,2S,3R,4S,5R,6S)-2-allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyl ester 
• 638203-39-1 (1R,2R,3R,4S,5S,6R)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexanol 
• 316806-88-9 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol 
• 637329-53-4 Acetic acid (1R,2S,3R,4S,5R,6S)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyl ester 

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