Đầu trang>Giải pháp | Danh mục công nghệ> 2 Suzuki-Miyaura coupling reaction using link bong88 com catalyst
- You can use zero-valent nickel catalysts, such as link bong88 com(COD)2, or divalent nickel catalysts, which are cheaper and easier to use
- By utilizing the high reactivity of link bong88 com catalysts, the reaction can be carried out under milder conditions Therefore, it is possible to react even with thermally unstable compounds In addition, even compounds that are prone to racemization do not impair optical purity
- Inexpensive leaving groups such as chloride, tosylate, and mesylate can be used (Pd catalyst has poor reactivity and is difficult to use)
- Việc loại bỏ link bong88 com khỏi sản phẩm phản ứng rất dễ dàng Provides a solution to residual metal problems without special refining
- The reaction proceeds even if there is an unprotected amino group on the reaction substrate
- Buchwald type amination does not proceed
- There is no need to worry about residual link bong88 com in the reaction product
- We quickly find the optimal catalyst system for your compound through rapid reaction system screening
- Loài kim loại (link bong88 com, Pd)
- Các phối tử
- Cơ sở
- link bong88 com(COD)2, Pd(PPh3)4
- We have extensive experience in manufacturing boronic acids and boronic acid esters, and possess unique technology and know-how By collectively manufacturing boronic acids, we will simplify the supply chain related to your Suzuki coupling
