110205-68-0

Upstream product

• 100-44-7 benzyl chloride 
• 93125-77-0 (2R,3R,4R,5S)-1,3,4-tris(benzyloxy)hept-6-ene-2,5-diol 
• 79258-18-7 (2R,3R,4R,5S)-1,3,4,5-tetrakis(benzyloxy)hept-6-en-2-ol 

Downstream Products

• 669015-46-7 Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine 
• 1193132-10-3 (3aS,4S,5R,6R,6aR)-1-benzyl-4,5,6-tris(benzyloxy)-6a-(benzyloxymethyl)hexahydro-1H-cyclopenta[c]isoxazole 
• 74645-52-6 (1L)-(1,3,4/2)-4-acetamido-1,2,3-tri-O-acetyl-4-[(acetoxy)methyl]cyclohex-5-ene-1,2,3-triol 
• 176540-16-2 (2R,3R,4S,5S,6S)-1-Benzyl-3,4,5-tris-benzyloxy-2-benzyloxymethyl-6-iodomethyl-piperidine 
• 227930-76-9 (1L)-(1,3,4/2)-1,2,3-tri-O-benzyl-4-[(benzyloxycarbonyl)amino]-6-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3-triol 
• 227930-75-8 (1D)-(1,3,4/2)-1,2,3-tri-O-benzyl-4-C-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3,4-tetrol 
• 227930-72-5 (1D)-(1,3,4/2)-1,2,3-tri-O-benzyl-4-C-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3,4-tetrol 
• 128500-09-4 (1D)-(1,3/2,4)-1,2,3-tri-O-benzyl-4-C-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3,4-tetrol 
• 106988-93-6 1L-(1,2,4/3)-1,2,3,4-tetra-O-benzyl-1-C-(benzyloxymethyl)-5-cyclohexen-1,2,3,4-tetrol 
• 118968-04-0 (1L)-(,3,4/2)-4-acetamido-1,2,3-tri-O-benzyl-4-[(benzyloxy)methyl]cyclohex-5-ene-1,2,3-triol 
• 38231-86-6 valienamine 
• 227930-71-4 3,4,5-tri-O-benzyl-6-C-[(benzyloxy)methyl]-1,2,7,8-tetradeoxy-D-gluco-octa-1,7-dienitol 
• 176540-15-1 Benzyl-((1R,2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine 

Relevant academic research and scientific papers

Synthesis and biological evaluation of the first example of an eight-membered iminoalditol

The synthesis of the first examples of eight-membered iminoalditols has been achieved from 2,3,4,6-tetra-O-benzyl-D-glucopyranose by way of a ring-closing metathesis. The (2R,3R,4R,5S)-2-hydroxymethyl-azocane-3,4,5-triol (3a), which has the D-gluco config

First total synthesis of (+)-hyacinthacine A2

The first synthesis of (+)-hyacinthacine A2 has been achieved in six steps from 2,3,5-tri-O-benzyl-D-arabinofuranose in an overall yield of 11%. The structure of this natural product was thus unambiguously established as (1R,2R,3R,7aR)-1,2-dihydroxy-3-hydroxymethylpyrrolizidine

Intramolecular ketonitrone-olefin cycloaddition reaction: direct and stereocontrolled synthesis of nitrogenated quaternary centered aminocyclopentitols as galactosidase inhibitors

Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation of ketonitrone-olefin cycloaddition reaction as a key step has been accomplished in a stereocontrolled manner. The target molecules were found to be modera

Stereospecific synthesis of eight-membered polyhydroxy carbocycles via TIBAL-promoted claisen rearrangement

The stereoselective synthesis of novel eight-membered polyhydroxy carbocycles was achieved from D-glucose via mercuriocyclization and triisobutylaluminum (TIBAL)-promoted Claisen rearrangement. Along with rearrangement, TIBAL also promoted debenzylation a

An efficient synthetic approach to aza-C-glycosyl compounds. Application to the synthesis of an aza-C-disaccharide

The NIS-mediated cyclization of aminoheptenitols 5-8 (prepared in three steps from tetra-O-benzyl-D-hexopyranoses) provided 1,2,6-trideoxy-2,6-imino-l-iodoheptitol derivatives 9-12, respectively, highly stereoselectively and in high yield. The "α-D-glucoα