The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.Application In Synthesis of 1,5-Diphenylpenta-1,4-dien-3-one, Name is 1,5-Diphenylpenta-1,4-dien-3-one, molecular formula is C17H14O, Application In Synthesis of 1,5-Diphenylpenta-1,4-dien-3-one. In a Article, authors is Min, Deng£¬once mentioned of Application In Synthesis of 1,5-Diphenylpenta-1,4-dien-3-one
Fe-catalyzed dithiane radical induced C?S bond activation?addition to alpha, beta-unsaturated ketones
An efficient and clean strategy to construct organosulfur compounds has been developed via a Fe-catalyzed dithiane C?S bond activation/addition process with alpha, beta-unsaturated ketones. This C?S activation protocol exhibits excellent reactivities, and up to 92% yield of the corresponding thioether-thioester derivatives could be obtained under the mild conditions, allowing the ready preparation of a number of synthetically valuable S-linked conjugates. (Figure presented.).
Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. Keep reading other articles of 538-58-9! Application In Synthesis of 1,5-Diphenylpenta-1,4-dien-3-one
Reference£º
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate