16-Sep-2021 News Extracurricular laboratory:new discovery of 15861-24-2

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 15861-24-2, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 15861-24-2

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent, Product Details of 15861-24-2, Which mentioned a new discovery about 15861-24-2

A new and efficient copper-catalyzed C3 aryl- and heteroarylselenation of indoles employing selenium powder has been developed. The advantages of this chemistry involve the use of cheap selenating reagents, tolerance of a variety of functional groups, and practicality. In addition, this protocol has been further elaborated in an intramolecular phenylselenation of a (hetero) aryl C-H bond to construct an important motif of benzoselenopheno[3,2-b]indole. A preliminary mechanism study suggests that the reaction starts with a Ullman-type selenation between aryl iodides and selenium, followed by an oxidative cross-coupling with indole. The utility of this method has been demonstrated in an efficient gram-scale synthesis and an application to the synthesis of tubulin polymerization inhibitor.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 15861-24-2, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 15861-24-2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles