The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5-Methylfuran-2(3H)-one( cas:591-12-8 ) is researched.Formula: C5H6O2.Romaniszyn, Marta; Gronowska, Katarzyna; Albrecht, Lukasz published the article 《Remote Functionalization of 4-(Alk-1-en-1-yl)-3-Cyanocoumarins via the Asymmetric Organocatalytic 1,6-Addition》 about this compound( cas:591-12-8 ) in Advanced Synthesis & Catalysis. Keywords: dihydrofuranyl ethyl oxo chromene carbonitrile preparation diastereoselective enantioselective regioselective; alkenyl cyanocoumarin furanone organocatalytic addition. Let’s learn more about this compound (cas:591-12-8).
An organocatalytic 1,6-addition using 4-(alk-1-en-1-yl)-3-cyanocoumarins as acceptors was developed. Dienolates derived from 5-substituted-furan-2(3H)-ones have been employed as pronucleophiles, therefore, enabling the synthesis of hybrid mols. bearing two biol. relevant units I [R = H, 7-MeO, 6-Br, etc.; R1 = Me, allyl, Ph, etc.; R2 = H, Me; R3 = H, Me]. Appropriate design of substrates and the application of quinine-derived catalyst resulted in very good site-selectivity as well as chem. and stereochem. efficiency of the process.
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Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia