Chemical Research Letters, May 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. catalysts provide a surface to which reactants bind. In an article, author is Patra, Sanjib K., once mentioned the application of 179324-87-9, Name is (R)-BoroLeu-(+)-Pinanediol trifluoroacetate. Now introduce a scientific discovery about this category, Safety of (R)-BoroLeu-(+)-Pinanediol trifluoroacetate.
An aldol-like addition of acetone to 2-methyl-1,8-naphthyridine and 2,3-dimethyl-1,8-naphthyridine mediated by a [Ru-2(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 [Ru-2(CO)(4)(L1)(2)][X](2) (2, X = BF4; 2a, X = OTf), [Ru-2(CO)(4)(L2)(2)][BF4](2) (3), and [Ru-2(CO)(4)(L3)(2)][BF4](2) (4) are reported here.
The dynamic chemical diversity of the numerous elements, ions and molecules that constitute the basis of life provides wide challenges and opportunities for research. In my other articles, you can also check out more blogs about 179324-87-9. Safety of (R)-BoroLeu-(+)-Pinanediol trifluoroacetate.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem