638203-45-9

Upstream product

• 100-39-0 benzyl bromide 
• 331679-26-6 2,3-O-(D-1,7,7-trimethylbicyclo[2.2.1]hept-6-ylidene)-D-myo-inositol 
• 100-44-7 benzyl chloride 
• 87-89-8 D-myo-inositol 
• 149713-85-9 4,6-di-O-benzyl-myo-inositol 
• 98510-25-9 meso-4,6-di-O-benzyl-D-myo-inositol-1,3,5-O-orthoformate 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 

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 
• 637329-52-3 Acetic acid (1S,2S,3R,4R,5S,6R)-2,3,4,5-tetrakis-benzyloxy-6-trifluoromethanesulfonyloxy-cyclohexyl ester 
• 638203-33-5 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol 
• 637329-56-7 Acetic acid (1R,2S,3R,4S,5R,6S)-2-allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyl ester 
• 637329-53-4 Acetic acid (1R,2S,3R,4S,5R,6S)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-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 
• 177471-67-9 3,4,5,6-tetra-O-benzyl-2-deoxy-scyllo-inosose 
• 177471-66-8 L-1-deoxy-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 149656-37-1 D-2-deoxy-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 

Relevant academic research and scientific papers

Advances in analysis and synthesis of myo-inositol-derivatives through resolution by crystallisation

A simple method for the preparation of both enantiomers of tetra-O-benzyl-myo-inositol is presented. This method is based on the resolution of stereoisomers by crystallisation. Starting with the known synthesis of four diastereomers using d-camphor dimeth

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

Concise syntheses of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3- PIP), 5-phosphate (5-PIP), and 3,5-bisphosphate (3,5-PIP2)

Highly efficient, asymmetric total syntheses of the title phospholipids as well as short chain and crosslinkable aminoether analogs were achieved in five to seven steps from a readily available myo-inositol derivative. (C) 2000 Elsevier Science Ltd.