114144-68-2

Upstream product

• 26291-75-8 (R)-1-((3aR,5S,6R,6aR)-2,2,6-trimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 56982-95-7 (3aR,5S,6R,6aR)-2,2,6-trimethyl-5-((R)-oxiran-2-yl)tetrahydrofuro[2,3-d][1,3]dioxole 
• 100-39-0 benzyl bromide 
• 114144-67-1 6-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-allofuranose 

Downstream Products

• 114171-76-5 6-O-benzyl-3,5-dideoxy-1,2-O-isopropylidene-3-C-methyl-5-methylene-α-D-ribo-hexafuranose 
• 184964-71-4 (1R,3S,4R,5R)-3-[(E/Z)-1-benzyloxymethyl-2-ethoxycarbonylethenyl]-4-methyl-7,7-dimethyl-2,6,8-trioxabicyclo[3.3.0]octane 
• 552848-95-0 C₁₈H₂₅NO₅ 
• 145451-97-4 (3R,4S,5R,1'S)-4-hydroxy-5-(1'-hydroxy-2'-methylpropyl)-3-methylpyrrolidin-2-one-5-carboxylic acid 
• 133343-34-7 Lactacystin 
• 166541-05-5 (3R,4S,5R)-5-benzyloxymethyl-4-hydroxy-3-methyl-5-vinyl-2-pyrrolidinone 
• 184964-73-6 (1R,3S,4R,5R)-3-[(E/Z)-1-benzyloxymethyl-3-hydroxy-1-propenyl]-4-methyl-7,7-dimethyl-2,6,8-trioxabicyclo[3.3.0]octane 
• 199734-91-3 (3R,4S,5R)-5-benzyloxymethyl-4-(tert-butyldimethylsilyl)oxy-3-methyl-5-vinyl-2-pyrrolidinone 
• 184964-82-7 Formic acid (2R,3S,4R)-2-benzyloxymethyl-5-hydroxy-4-methyl-1-(2,2,2-trichloro-acetyl)-2-vinyl-pyrrolidin-3-yl ester 
• 184964-75-8 2,2,2-Trichloro-acetimidic acid (E)-4-benzyloxy-3-((3aR,5S,6R,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-but-2-enyl ester 
• 184964-77-0 (1R,3S,4R,5R)-3-[(1RS)-1-benzyloxymethyl-1-trichloroacetylamino-2-propenyl]-4-methyl-7,7-dimethyl-2,6,8-trioxabicyclo[3.3.0]octane 
• 114144-81-9 3,5-dideoxy-1,2-O-isopropylidene-6-(4-methoxybenzyl)-3,5-dimethyl-β-L-talofuranose 
• 114144-83-1 2,4-dideoxy-3-O-formyl-5-O-(4-methoxybenzyl)-2,4-di-C-methyl-L-lyxose 
• 114144-72-8 6-O-benzyl-3,5-dideoxy-1,2-O-isopropylidene-3,5-di-C-methyl-β-L-talofuranose 

Relevant academic research and scientific papers

Intra- and intermolecular 1,3-dipolar cycloaddition of sugar ketonitrones with mono-, di-, and trisubstituted dipolarophiles

The 1,3-dipolar cycloaddition of sugar ketonitrones is a useful synthetic procedure to build up nitrogenated quaternary centers in terms of scope (substrate, dipolarophile, inter- and intramolecular versions), yield, and regio- and stereoselectivity. The

Stereoselective total synthesis of (+)-lactacystin from D-glucose

The chiral and stereoselective synthesis of (+)-lactacystin 1, the first non-protein neurotrophic factor having an α,α-disubstituted α- amino acid structure, is described. The highly functionalized γ- lactam portion possessing a tetra-substituted carbon w

Total Synthesis of (+)-Lactacystin from D-Glucose

The chiral and stereoselective synthesis of (+)-lactacystin 1, the first non-protein neurotrophic factor, is described; the γ-lactam portion possessing a quaternary carbon in 1 was constructed stereoselectively from D-glucose using the allylic trichloroac