New explortion of (S)-( )-5-Oxo-2-tetrahydrofurancarboxylic 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 21461-84-7

Reference of 21461-84-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.21461-84-7, Name is (S)-( )-5-Oxo-2-tetrahydrofurancarboxylic Acid, molecular formula is C5H6O4. In a Article£¬once mentioned of 21461-84-7

Diastereocontrol in Glycosylation Reactions: Synthesis of beta-D and beta-L Dideocytidine Analogues

Expeditious and diastereoselective total syntheses of the antiviral agents, beta-L-ddC, beta-L-5FddC and beta-D-5FddC have been achieved in four steps from commercially available R-(-)-5-oxo-2-tetrahydrofurancarboxylic and its 2S isomer respectively.

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Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem