35522-89-5

Usage

Uses

Used in Pharmaceutical Industry:
(3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole-5-carboxylic acid is used as a potential pharmaceutical compound for its unique molecular structure and chemical properties. Further research and analysis are required to fully understand its potential therapeutic applications and benefits.
Used in Chemical Industry:
(3aS,5R,6S,6aS)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole-5-carboxylic acid is used as a chemical intermediate or building block in the synthesis of other complex organic compounds. Its unique structure and functional groups may offer advantages in the development of new materials and chemical processes.

InChI:InChI=1/C8H12O6/c1-8(2)13-5-3(9)4(6(10)11)12-7(5)14-8/h3-5,7,9H,1-2H3,(H,10,11)/t3-,4-,5+,7+/m0/s1

Upstream product

• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 18549-40-1 1,2-O-isopropylidene-α-D-glucofuranose 

Relevant academic research and scientific papers

Oxidation of Primary Alcohols and Aldehydes to Carboxylic Acids via Hydrogen Atom Transfer

The oxidation of primary alcohols and aldehydes to the corresponding carboxylic acids is a fundamental reaction in organic synthesis. In this paper, we report a new chemoselective process for the oxidation of primary alcohols and aldehydes. This metal-free reaction features a new oxidant, an easy to handle procedure, high isolated yields, and good to excellent functional group tolerance even in the presence of vulnerable secondary alcohols and tert-butanesulfinamides.

PROCESS FOR THE PREPARATION OF SOTAGLIFLOZIN

Sotagliflozin may be prepared using schemes and intermediates disclosed herein. Sotagliflozin may be incorporated into pharmaceutical dosage forms for treatment of diabetes.

Catalytic oxidation of D-glucose derivatives with oxygen in alkali solutions in the presence of copper phenanthroline complexes

Features of oxidation of model compounds, 1-O-methyl-D-glycoside and 1,2-O-isopropylidene-D-glucose, with oxygen in aqueous alkali solutions were studied to determine probable reaction centers in starch oxidation.

Selective oxidation of monosaccharide derivatives to uronic acids

Primary hydroxyl groups in partially protected monosaccharide derivatives were selectively oxidised to carboxylic acids using sodium hypochlorite in the presence of catalytic amounts of 2,2,6,6-tetramethyl-1-piperidinyl oxy, free radical (TEMPO). Acetal,

Oxidation of partially protected carbohydrates at the nickel hydroxide electrode

Primary hydroxy groups in pyranoses are oxidized in excellent yields to the corresponding carboxylic acids. In furanose 3 the yield of acid is only moderate. Secondary hydroxy groups are inert, aside from lactols. The different reactivity of secondary and primary hydroxy groups allows the chemoselective oxidation of 8 and 10.