53717-00-3

Usage

Uses

Used in Organic Synthesis:
(2S,3R,4S,5R,6R)-5-Hydroxy-2-methoxy-6-((trityloxy)methyl)tetrahydro-2H-pyran-3,4-diyl diacetate is used as a building block for the synthesis of complex organic molecules. Its unique structure allows for the formation of various chemical bonds and reactions, making it a valuable component in the creation of new compounds.
Used in Medicinal Chemistry:
(2S,3R,4S,5R,6R)-5-Hydroxy-2-methoxy-6-((trityloxy)methyl)tetrahydro-2H-pyran-3,4-diyl diacetate is used as a potential pharmaceutical candidate due to its unique structure and functional groups. It may be utilized in the development of new drugs or as a key intermediate in the synthesis of bioactive molecules.
Used in Chemical Research:
(2S,3R,4S,5R,6R)-5-Hydroxy-2-methoxy-6-((trityloxy)methyl)tetrahydro-2H-pyran-3,4-diyl diacetate is used as a subject of study in chemical research to explore its properties, reactivity, and potential applications. Its stereospecific configuration and functional groups make it an interesting compound for understanding various chemical phenomena and reactions.

Upstream product

• 76-83-5 trityl chloride 
• 29868-42-6 methyl 2,3-di-O-acetyl-α-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 18311-26-7 methyl 6-O-trityl-α-D-glucopyranoside 
• 76-84-6 triphenylmethyl alcohol 

Downstream Products

• 31505-47-2 methyl 2,3-di-O-acetyl-4-O-(methylsulfonyl)-6-O-triphenylmethyl-α-D-glucopyranoside 
• 5540-29-4 methyl 3,4-anhydro-6-O-triphenylmethyl-α-D-galactopyranoside 
• 142504-76-5 methyl 3,4-anhydro-2-O-methyl-6-O-triphenylmethyl-α-D-galactopyranoside 
• 142504-78-7 methyl 3,4-anhydro-2-O-tetrahydropyranyl-6-O-triphenylmethyl-α-D-galactopyranoside 

Relevant academic research and scientific papers

Mild benzhydrylation and tritylation of saccharidic hydroxyls promoted by acid washed molecular sieves

Commercially available 4 ? acid washed molecular sieves (AW 300 MS) promote the protection of primary and secondary saccharidic alcohols through a dehydration mechanism and in the absence of any strong protic or Lewis acid.

Diazepinium perchlorate: a neutral catalyst for mild, solvent-free acetylation of carbohydrates and other substances

Diazepinium perchlorate, an essentially neutral organic salt possessing excellent stability, has been found to be well suited for the acetylation of free as well as partially protected sugars, phenols, thiophenols, thiols and other alcohols as well as amines. The diazepinium perchlorate-catalyzed acetylation is mild, organic and solvent-free and leaves acid sensitive protecting groups such as TBDMS/TBDPS/Tr ethers and isopropylidene/benzylidene acetals present on a substrate unaffected. Regioselective hydroxyl protection in partially protected carbohydrate derivatives/polyhydroxylic compounds was possible and was proved to be a convenient time-saving alternative to the conventional synthesis of such compounds. Easy preparation of the catalyst, mild reaction conditions and an environmentally benign protocol are some of the notable features of this reaction. The results obtained on the acetylation of phenols and thiophenols could be rationalized through their local nucleophilicity index obtained from DFT calculations.

Chemical modification of the sugar part of methyl acarviosin: Synthesis and inhibitory activities of nine analogues

Nine analogues of methyl acarviosin (1), the core structure of acarbose and its homologues, the 6-hydroxy-(2), 6-azido-(3), 6-amino-(4), 6-acctamido-(5), 6-methoxy-(6), 6-hydroxy-2-O-methyl-(8), and 6-hydroxy-3-O-methyl derivatives (9), including the 5-me