Extracurricular laboratory:new discovery of 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.Application of 1569-16-0

Application 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

An aldol-like addition of acetone to 2-methyl-1,8-naphthyridine and 2,3-dimethyl-1,8-naphthyridine mediated by a [Ru2(CO) 4]2+ core at room temperature affords the C-C-coupled compounds 2-methyl-1-(1,8-naphthyridin-2-yl)propan-2-ol (L1) and 2-methyl-1-(3-methyl-1,8-naphthyridin-2-yl)propan-2-ol (L2). A similar reaction with methyl ethyl ketone and 2-methyl-1,8-naphthyridine affords 2-methyl-1-(1,8-naphthyridin-2-yl)butan-2-ol (L3). The syntheses and structures of [Ru2(CO)4(L1)2][X]2 (2, X = BF4; 2a, X = OTf), [Ru2(CO)4(L 2)2][BF4]2 (3), and [Ru 2(CO)4(L3)2][BF4]2 (4) are reported here.

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.Application of 1569-16-0

Reference£º
1,363-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N357 – PubChem