177471-67-9

Upstream product

• 177471-65-7 DL-1-O-tosyl-3,4,5,6-tetra-O-benzylmyoinositol 
• 128387-20-2 L-1,2-O-isopropylidene-myo-inositol 
• 638203-33-5 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol 
• 177471-66-8 L-1-deoxy-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 131233-67-5 1,4,5,6-tetra-O-benzyl-2,3-isopropylidene-sn-myo-inositol 
• 100-39-0 benzyl bromide 
• 638203-45-9 C₄₄H₅₀O₆ 
• 28140-40-1 1,4,5,6-tetra-O-benzyl-myo-inositol 
• 87-89-8 D-myo-inositol 

Downstream Products

• 222055-98-3 tri-O-benzyl-2,6-dideoxy-scyllo-inosose 
• 149656-37-1 D-2-deoxy-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 177471-66-8 L-1-deoxy-3,4,5,6-tetra-O-benzyl-myo-inositol 
• 78963-40-3 2L-(2,4/3,5)-2,3,4,5-tetrahydroxycyclohexan-1-one 

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

Convenient synthesis of 2-deoxy-scyllo-inosose and 2-deoxy-scyllo-inosamine: Two key intermediates on the biosynthetic pathway to aminoglycoside antibiotics

2-Deoxy-scyllo-inosose 1 and 2-deoxy-scyllo-inosamine 2 are two of the key intermediates on the biosynthetic pathway to 2-deoxystreptamine-containing aminoglycoside antibiotics. Convenient syntheses of 1, 2 and tritium-labelled 2 via stereoselective deoxy