Some scientific research about 1,5-Diphenylpenta-1,4-dien-3-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 538-58-9

Synthetic Route of 538-58-9, Research speed reading in 2021. We’ll be discussing some of the latest developments in chemical about CAS: 538-58-9 In a document type is Article, and a compound is mentioned, 538-58-9, Name is 1,5-Diphenylpenta-1,4-dien-3-one, introducing its new discovery.

The reaction of selenium monoketo ylides with the dibenzylidene derivatives of ketones (acetone, cyclopentanone, cyclohexanone) only takes place at one double bond of the dienone by a mechanism of the <1+2>-cycloaddition type with the formation of two isomeric cyclopropyl ketones.In the case of the dibenzylidene derivative of bicyclo<3.3.1>nonan-3-one the type of reaction, i.e., <1+2>– or <1+4>-cycloaddition, is determined by the direction of attack by the selenonium ylide (axial or equatorial).

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 538-58-9

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate