Application In Synthesis of Phenyl(pyridin-2-yl)methanone. Recently I am researching about C-H BONDS; COUPLED ELECTRON-TRANSFER; DIRECT ARYLATION; ACTIVATION; CATALYSIS; FUNCTIONALIZATION; ALDEHYDES; HALIDES; MERGER, Saw an article supported by the National Research Foundation [NRF2016NRF-NSFC002-005]; Ministry of Education, SingaporeMinistry of Education, Singapore [MOE 2013-T3-1-002]; MOE Tier 1 grantMinistry of Education, Singapore [RG 111/18]; Agency for Science, Technology and Research (A*STAR), AME IRG grantAgency for Science Technology & Research (ASTAR) [A1783c0002]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Vu, MD; Das, M; Guo, AX; Ang, ZE; Dokic, M; Soo, HS; Liu, XW. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone
Being a handle for synthesizing quaternary carbon centers and olefins, together with ubiquitous appearance in organic building blocks, makes tertiary alcohols valuable targets in synthesis. However, traditional syntheses of these alcohols have faced several challenges including the employment of functionalized reactive reagents, undesirable side reactions, and decomposition of the alcohol products under harsh conditions. The paucity of a synthetic approach to bulky tertiary alcohols prompts our interest to develop a benign catalytic protocol to tackle the current issues. Here, we have successfully demonstrated the use of ketyl radicals in intermolecular cross radical-radical coupling, which has opened a different door for accessing complex tertiary alcohols. On the other hand, by starting from feedstock and naturally derived chemicals without any pre-activation, it would be superior to traditional methodologies in the industrial context.
Application In Synthesis of Phenyl(pyridin-2-yl)methanone. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem