Bernhard, Yann published the artcileOne-Pot Synthesis of 2,5-Disubstituted Furans through In Situ Formation of Allenes and Enolization Cascade, Product Details of C7H12O3, the main research area is furan preparation ketoacid enolization cyclization cascade.
A one-pot synthesis of 2,5-disubstituted furans from γ-ketoacids is reported. In situ formation of allenoates by action of chloroformate on carboxylic acid following by enolization of ketone affords furan derivatives by cyclization. The reaction was extended to a wide scope of ketoacids and phosphonium salts. This methodol. was applied on levulinic acid and derivatives, one of the biosourced platform chems.
European Journal of Organic Chemistry published new progress about Carboxylic acids Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 539-88-8 belongs to class esters-buliding-blocks, name is Ethyl 4-oxopentanoate, and the molecular formula is C7H12O3, Product Details of C7H12O3.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics