(2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Synthetic Route of C16H22O11
Stereoselective synthesis of novel thioglycosyl heterocycles was written by El Ashry, El Sayed H.;Awad, Laila F.;Abd Al Moaty, Mohamed N.;Ghabbour, Hazem A.;Barakat, Assem. And the article was included in Journal of Molecular Structure in 2018.Synthetic Route of C16H22O11 This article mentions the following:
In this work, the synthesis of novel 1,2,4-triazole thioglycoside heterocycles, e.g. I, were achieved by the reaction of 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose and galactopyranose with 4-((4-arylidene)amino)-5-methyl-1,2,4-triazole-3-thiol derivatives, e.g. II, in the presence of boron trifluoride etherate (BF3·Et2O) as a promoter under nitrogen in CH2Cl2. Exclusive β-stereoselectivity of the formed glycosidic bond was confirmed by X-ray anal. of I as well as its spectral data. Different stereoselectivities were observed when the acceptor having an ortho phenolic OH group, was coupled with the donors, under the same reaction conditions. Similarly, treatment of a mixture of 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose and the thiol acceptor II afforded the β-thio-ribofuranosides. The β-stereoselectivity of the reaction was confirmed by 1H, 13C, 1H-1H 2D, and 1H-13C 2D NMR spectral anal. In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4Synthetic Route of C16H22O11).
(2S,3R,4S,5S,6R)-6-(Acetoxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate (cas: 4163-60-4) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Synthetic Route of C16H22O11
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics