18006-25-2

Usage

Uses

Used in Organic Synthesis:
3-O-Benzyl-5,6-di-O-acetyl-1,2-O-isopropylidene-a-D-glucofuranose is used as a building block for the synthesis of more complex molecules, leveraging its unique structure to create a variety of chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-O-Benzyl-5,6-di-O-acetyl-1,2-O-isopropylidene-a-D-glucofuranose is utilized as a protecting group for hydroxyl functional groups in carbohydrate chemistry, facilitating the development of new drug candidates and enhancing the synthesis process.
Used in Chemical Industry:
3-O-Benzyl-5,6-di-O-acetyl-1,2-O-isopropylidene-a-D-glucofuranose is employed in the chemical industry for its versatility in creating diverse applications, contributing to the advancement of chemical processes and products.

InChI:InChI=1/C20H26O8/c1-12(21)23-11-15(25-13(2)22)16-17(24-10-14-8-6-5-7-9-14)18-19(26-16)28-20(3,4)27-18/h5-9,15-19H,10-11H2,1-4H3

Upstream product

• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 108-24-7 acetic anhydride 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 106221-10-7 Acetic acid (R)-1-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-but-3-enyl ester 
• 106221-02-7 [(Z)-3-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-trimethyl-silane 
• 106221-07-2 (R)-1-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-prop-2-en-1-ol 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 50-99-7 D-glucose 
• 100-39-0 benzyl bromide 
• 64656-76-4 Natrium-Verbindung der O¹,O²;O⁵,O⁶-Diisopropyliden-α-D-glucofuranose 

Downstream Products

• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 39798-98-6 O³-benzyl-O¹,O²-isopropylidene-O⁵,O⁶-dimethyl-α-D-glucofuranose 
• 42926-89-6 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose 
• 1218918-94-5 acetic acid (1R,2R,3R,4S,5S)-2-acetoxy-1-(5-allyl-3-benzyloxy-4-hydroxy-tetrahydrofuran-2-yl)-ethyl ester 
• 35781-78-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 22331-18-6 O³-benzyl-O¹,O²-isopropylidene-O⁵,O⁶-bis-(toluene-4-sulfonyl)-α-D-glucofuranose 
• 18006-29-6 O⁶-benzoyl-O³-benzyl-O¹,O²-isopropylidene-O⁵-(toluene-4-sulfonyl)-α-D-glucofuranose 
• 781657-62-3 phenyl 2,4,6-tri-O-acetyl-1-thio-α/β-L-idopyranose 
• 781657-65-6 Acetic acid (2R,4aS,7R,8S,8aR)-8-benzyloxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 781657-64-5 (2R,4aS,7R,8R,8aR)-8-Benzyloxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 781657-63-4 phenyl 3-O-benzyl-1-thio-L-idopyranoside 
• 37776-17-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-β-L-idofuranose 
• 118711-49-2 1,2,4,6-tetra-O-acetyl-3-O-benzyl-L-idopyranoside 
• 84563-90-6 6-O-acetyl-3-O-benzyl-1,2-O-isopropylidene-5-O-methanesulfonyl-α-D-glucofuranose 

Relevant academic research and scientific papers

SYNTHESIS OF SOME L-IDOSE DERIVATIVES

The synthesis of 3-O-benzyl and 3-O-mesyl-1,2-O-isopropylidene-β-L-idofuranose has been effected on the basis of the intramolecular nucleophilic exchange of a mesyloxy group at C5 in derivatives of 1,2-O-isopropylidene-α-D-glucofuranose.It has

Synthesis of a polysulfated heparin degradation product

Two suitable methods for the synthesis of the heparin degradation product 2,5-anyhydro-3-O-(α-L-ido-pyranosyluronate)-D-mannitol hexa O-sulfate are reported. The synthesis pathways start from D-glucose and D-glucosamine.

ON THE COMMUNICATION OF CHIRALITY FROM FURANOSE AND PYRANOSE RINGS TO MONOSACCHARIDE SIDE CHAINS: ANOMALOUS RESULTS IN THE GLUCOSE SERIES

The reactions of allyltrimethylsilane with dialdose derivatives occur, under catalysis by boron trifluoride etherate or titanium tetrachloride, with high stereoselectivity, thereby providing simple routes to the corresponding allyl carbinols.The sense of