120615-67-0

Upstream product

• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-ribo-3-hexulofuranose 
• 55533-85-2 3-O-benzyl-1,2:5,6-di-O-isopropylidene-3-C-methyl-α-D-glucofuranose 
• 35784-67-9 1,2:5,6-di-O-isopropylidene-3-C-methyl-α-D-glucofuranose 
• 53270-27-2 C₁₃H₂₀O₆ 
• 53270-26-1 (3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl[1,3]dioxolan-4-yl]-2,2,6-trimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 111138-00-2 C₂₀H₂₈O₆ 
• 100-39-0 benzyl bromide 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 35784-67-9 1,2;5,6-di-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 

Downstream Products

• 81841-44-3 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-α-D-ribopentodialdo-1,4-furanose 
• 99050-15-4 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropyliden-3-C-methyl-α-D-allo-hexofuranose 
• 110808-85-0 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-6-O-methylbenzoyl-α-D-allofuranose 
• 98003-97-5 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-5,6-ditosyloxy-α-D-allofuranose 
• 99050-12-1 3-O-Benzyl-1,2-O-isopropyliden-3-C-methyl-6-O-(p-tolylsulfonyl)-α-D-allo-hexofuranose 
• 64638-70-6 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-3-C-methyl-α-D-ribo-hexofuranose 
• 55533-90-9 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-3-C-methyl-β-L-talo-hexofuranose 
• 55533-89-6 5,6-Anhydro-3-O-benzyl-1,2-O-isopropyliden-3-C-methyl-β-L-talo-hexofuranose 
• 99050-26-7 (E)-4-O-Benzyl-4-C-methyl-5,6,7-tridesoxy-D-arabino-hept-5-enose-trimethylendithioacetal 
• 99050-16-5 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropyliden-3-C-methyl-5-O-(p-tolylsulfonyl)-α-D-allo-hexofuranose 
• 99050-13-2 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-3-C-methyl-α-D-allo-hexofuranose 
• 99050-14-3 3-O-Benzyl-5,6-didesoxy-1,2-O-isopropyliden-5-iod-3-C-methyl-β-L-talo-hexofuranose 
• 99050-17-6 3-O-Benzyl-5,6-didesoxy-1,2-O-isopropyliden-5-iod-3-C-methyl-α-D-allo-hexofuranose 
• 15397-12-3 2'-methyl-adenosine 

Relevant academic research and scientific papers

Synthesis and biophysical evaluation of 3′-Me-α-l-LNA - Substitution in the minor groove of α-l-LNA duplexes

The synthesis and biophysical evaluation of 3′-Me-α-l-LNA is reported. The synthesis of the nucleoside building block phosphoramidite was accomplished starting from diacetone glucose. The 3′-Me group was introduced in the desired configuration by hydride

Practical synthesis of a potent hepatitis C virus RNA replication inhibitor

A practical, efficient synthesis of 1, a hepatitis C virus RNA replication inhibitor, is described. Starting with the inexpensive diacetone glucose, the 12-step synthesis features a novel stereoselective rearrangement to prepare the key crystalline furanose diol intermediate. This is followed by a highly selective glycosidation to couple the C-2 branched furanose epoxide with deazapurine.

Anthracyclinones. Part 5. Synthesis of Some Anthracyclinones and 4-Hydroxyanthracyclinones containing a Tertiary Methyl Carbinol Function in Ring A from D-Glucose Precursors

Reaction of 3-C-Methyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose (8a) with leucoquinizarin (2,3,4a,9a-tetrahydroanthracene-1,4,9,10-tetraone) (1a) in alkaline solution followed by aerial oxidation gave mainly (5S)-3-C-methyl 1,2-O-isopropylid