Brief introduction of 5-Methylfuran-2(5H)-one

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 591-11-7. Product Details of 591-11-7.

Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics, Product Details of 591-11-7, 591-11-7, Name is 5-Methylfuran-2(5H)-one, SMILES is O=C1OC(C)C=C1, belongs to benzofurans compound. In a document, author is Zhu, Cheng-Zhi, introduce the new discover.

Rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole: synthesis of cyclopropa[cd]indole and benzofuran derivatives

A rhodium(ii)-catalyzed divergent intramolecular tandem cyclization of N- or O-tethered cyclohexa-2,5-dienones with 1-sulfonyl-1,2,3-triazole has been disclosed in this paper. When the connecting atom between the cyclohexa-2,5-dienone unit and the 1-sulfonyl-1,2,3-triazole moiety was a N-sulfonated group, a cyclopropanation of the olefinic unit in the cyclohexa-2,5-dienone moiety could take place, affording cyclopropa[cd]indole derivatives in moderate to good yields. This is the first example of the cyclopropanation of alpha-imino rhodium carbenes with electron-deficient intra-annular olefins. If the connecting linker was an oxygen atom, an oxy-Cope rearrangement could be triggered under similar reaction conditions, giving benzofuran derivatives. The reaction mechanisms have also been proposed along with a synthetic transformation.

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 591-11-7. Product Details of 591-11-7.

Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem