Synthetic Route of 1679-47-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1679-47-6, Name is 3-Methyldihydrofuran-2(3H)-one, molecular formula is C5H8O2. In a Article，once mentioned of 1679-47-6
A variety of monosubstituted gamma-lactols 4-6 were prepared in good yields by DIBAL reduction of the corresponding gamma-lactones 1-3.The monophenyl-substituted lactols 4b-6b were transformed into disubstituted tetrahydrofuran derivatives by replacement of the hydroxyl group by the alkyl residue of organometallic compounds used as nucleophiles.The diastereoselectivity of the substitution was found to depend strongly on the substitution pattern of the gamma-lactols.For the reaction of the 3- and 4-substituted derivatives 4b and 5b, respectively, good to excellent trans selectivity was observed, while the 5-substituted derivative reacted without any diastereoselectivity.These results were interpreted by means of the Felkin-Anh model. – Keywords: gamma-Lactone / Reduction / gamma-Lactol / Lewis acid / Tetrahydrofurans
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1679-47-6, and how the biochemistry of the body works.Synthetic Route of 1679-47-6
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem