New research progress on 51166-71-3 in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. In an article, author is Fan, Ming-Jin, once mentioned the application of 51166-71-3, Computed Properties of https://www.ambeed.com/products/51166-71-3.html, Name is 2,6-Di-O-methyl-β-cyclodextrin, molecular formula is C56H98O35, molecular weight is 1331.3563, MDL number is MFCD00011616, category is dioxole. Now introduce a scientific discovery about this category.
The reaction of phenols or 1,2-diphenols with activated alkynes took place smoothly and rapidly in the presence of a catalytic amount of 1,4-diazabicyclo[2.2.2] octane (DABCO) at room temperature and resulted in the formation of various alkenoic acid esters or 1,3-dioxole derivatives in excellent yields. The scope and limitations, together with a plausible mechanism of the reaction are disclosed in this paper.
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Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem