The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 1632-73-1, Name is 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol, SMILES is OC1C(C2)(C)CCC2C1(C)C, in an article , author is Lima, Fabio, once mentioned of 1632-73-1, Application In Synthesis of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol.
A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters
We report herein the use of a dual catalytic system comprising a Lewis base catalyst such as quinuclidin-3-ol or 4-dimethylaminopyridine and a photoredox catalyst to generate carbon radicals from either boronic acids or esters. This system enabled a wide range of alkyl boronic esters and aryl or alkyl boronic acids to react with electron-deficient olefins via radical addition to efficiently form C-C coupled products in a redox-neutral fashion. The Lewis base catalyst was shown to form a redox-active complex with either the boronic esters or the trimeric form of the boronic acids (boroxines) in solution.
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Reference:
Quinuclidine – Wikipedia,
,Quinuclidine | C7H13N | ChemSpider