Awesome Chemistry Experiments For 2-Methyl[1,8]-Naphthyridine

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1569-16-0, and how the biochemistry of the body works.Electric Literature of 1569-16-0

Electric Literature of 1569-16-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1569-16-0, Name is 2-Methyl[1,8]-Naphthyridine, molecular formula is C9H8N2. In a Article£¬once mentioned of 1569-16-0

A practical approach to the direct alpha-methylation of 1,8-naphthyridines under mild reaction conditions has been developed using simple and readily available DMSO as a convenient and environmentally friendly carbon source. This method is transition metal-free and highly chemoselective, shows good functional group tolerance, and uses DMSO as a methyl source, providing efficient and rapid access to an important compound class, 2-methyl-1,8-naphthyridines.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1569-16-0, and how the biochemistry of the body works.Electric Literature of 1569-16-0

Reference£º
1,350-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N344 – PubChem