Simple exploration of 3-Methylisoxazole-4-carboxylic acid

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 17153-20-7. Recommanded Product: 17153-20-7.

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , Recommanded Product: 17153-20-7, 17153-20-7, Name is 3-Methylisoxazole-4-carboxylic acid, molecular formula is C5H5NO3, belongs to Isoxazoles compound. In a document, author is MAEBA, I, introduce the new discover.

C-NUCLEOSIDES .21. SYNTHESIS OF ISOXAZOLE C-NUCLEOSIDE FROM FURANONE GLYCOSIDE VIA ENAMINONE GLYCOSIDE

Synthesis of the versatile and stable C-nucleoside precursor enaminone glycosides (3a,b) was achieved by reaction of furanone glycoside (1) with 2- and 4-aminophenols. Treatment of enaminone (3b) with hydroxylamine hydrochloride yielded 5-hydroxy-4,5-dihydroisoxazole(5), which on dehydration with toluene-p-sulfonic acid in benzene gave 5-(2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)isoxazole (6). Deblocking of compound (6) with sodium carbonate gave 5-(beta-D-ribofuranosyl)isoxazole (7).

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 17153-20-7. Recommanded Product: 17153-20-7.

Reference:
Isoxazole – Wikipedia,
,Isoxazole | C3H3NO – PubChem