Final Thoughts on Chemistry for 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 1632-73-1, Application In Synthesis of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol.

Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Zhou, Rong, once mentioned the application of 1632-73-1, Name is 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol, molecular formula is C10H18O, molecular weight is 154.2493, MDL number is MFCD00066640, category is quinuclidines. Now introduce a scientific discovery about this category, Application In Synthesis of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol.

Visible-Light-Mediated Metal-Free Hydrosilylation of Alkenes through Selective Hydrogen Atom Transfer for Si-H Activation

Although there has been significant progress in the development of transition-metal-catalyzed hydrosilylations of alkenes over the past several decades, metal-free hydrosilylation is still rare and highly desirable. Herein, we report a convenient visible-light-driven metal-free hydrosilylation of both electron-deficient and electron-rich alkenes that proceeds through selective hydrogen atom transfer for Si-H activation. The synergistic combination of the organophotoredox catalyst 4CzIPN with quinuclidin-3-yl acetate enabled the hydrosilylation of electron-deficient alkenes by selective Si-H activation while the hydrosilylation of electron-rich alkenes was achieved by merging photoredox and polarity-reversal catalysis.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 1632-73-1, Application In Synthesis of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol.

Reference:
Quinuclidine – Wikipedia,
,Quinuclidine | C7H13N | ChemSpider