108713-89-9

Upstream product

• 225797-51-3 (2R,3R,4R)-2,3,4-Trihydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxy]-pentanal 
• 100-39-0 benzyl bromide 
• 108713-87-7 5-O-trityl-D-ribose diethyl dithioacetal 
• 7152-47-8 D-ribose diethyl dithioacetal 
• 50-69-1 D-ribose 
• 105265-81-4 C₄₉H₅₂O₄S₂ 
• 117325-94-7 5-O-[(4-Methoxyphenyl)diphenylmethyl]-2,3,4-tris-O-(phenylmethyl)-D-ribose-diethyldithioacetal 

Downstream Products

• 112400-03-0 C₄₃H₄₆N₂O₈S₂ 
• 117325-96-9 2,3,4-Tris-O-(phenylmethyl)-5-O-(trimethylacetyl)-D-ribitol 
• 124077-36-7 1-O-β-D-Ribofuranosyl-5-O-(trimethylacetyl)-2,3,4-tris-O-(phenylmethyl)-D-ribitol 
• 117326-02-0 5-O-[(1,1-Dimethylethyl)dimethylsilyl]-2-O-[(phenylmethoxy)methyl]-β-D-ribofuranosyl-2,3,4-tris-O-(phenylmethyl)-D-ribitol 
• 117326-00-8 2,2-Dimethyl-propionic acid (2R,3S,4S)-2,3,4-tris-benzyloxy-5-((2R,3R,4R,5R)-3-benzyloxymethoxy-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yloxy)-pentyl ester 
• 117325-95-8 2,3,4-Tris-O-(phenylmethyl)-5-O-(trimethylacetyl)-D-ribose diethyldithioacetal 
• 233275-52-0 2,3,4-tri-O-benzyl-5-O-methanesulfonyl-D-ribose diethyl dithioacetal 
• 1607820-87-0 2,3,4-tri-O-benzyl-1-(N-benzyloxy-N-formylamino)-1,5-dideoxy-5-iodo-D-ribitol 
• 1607820-59-6 2,3,4-tri-O-benzyl-1-(N-benzyloxy-N-formylamino)-1-deoxy-5-oxo-D-ribitol 
• 1606161-71-0 phosphoric acid dibenzyl ester (2R,3S,4S)-2,3,4-tris-benzyloxy-5-(benzyloxy-formyl-amino)pentyl ester 
• 1606161-70-9 N-benzyloxy-N-((2S,3S,4R)-2,3,4-tris-benzyloxy-5-hydroxypentyl)formamide 
• 1606161-69-6 N-benzyloxy-N-((2S,3S,4R)-2,3,4-tris-benzyloxy-5-triisopropylsilanyloxy-pentyl)-formamide 
• 1607821-59-9 C₄₈H₅₂NO₈P 
• 1607821-00-0 N-benzyloxy-N-((25,35,4R)-2,3,4-tris-benzyloxy-5-hydroxy-1-trityloxymethylpentyl)formamide 

Relevant academic research and scientific papers

Samarium(II) iodide mediated intramolecular homelytic substitution at selenium: Preparation of 5-seleno-D-pentopyranose sugars from common pentose starting materials

Treatment of 2,3,4-tri-O-benzyl-5-benzylseleno-5-deoxyribose (9) with samarium(II) iodide in THF affords 2,3,4-tri-O-benzyl-5-deoxy-5-seleno-D- ribopyranose (10) in 50% isolated yield in a process most likely involving intramolecular homolytic substitutio

SYNTHESIS OF FRAGMENTS OF THE CAPSULAR POLYSACCHARIDE OF HAEMOPHILUS INFLUENZAE TYPE B

The synthesis of fragments, comprising two and four repeating units, of the title polysaccharide is described.

A Novel Transformation of Four Aldoses to Some Optically Pure Pseudohexopyranoses and a Pseudopentofuranose, Carboxylic Analogues of Hexopyranoses and Pentofuranose. Synthesis of Derivatives of (1S,2S,3R,4S,5S)-, (1S,2S,3R,4R,5S)-, (1R,2R,3R,4R,5S)-, (1S,

Knoevenagel reactions with dimethyl malonate of the suitably protected acylic aldehydes 6, 20, 34, and 46, which were prepared from D-ribose, D-xylose, D-arabinose, and D-erythrose, respectively, proceeded smoothly to provide α,β-unsaturated diesters 7, 2

A NEW TRANSFORMATION OF ALDOSE DERIVED SYNTHONS TO PSEUDO-HEXOPYRANOSE OR PSEUDO-PENTOFURANOSE DERIVATIVES

The D-ribose or D-erythrose derived acyclic synthon, which possesses a 2-malonyl carbon chain at C-1 position, was cyclized stereoselectively to a six- or five-membered carbocycle.Those carbocycles were converted into pseudo-β-L-mannopyranose derivatives