ReviewSpecial Issue: Transition-Metal CatalysisChelation-Assisted Nickel-Catalyzed C−H Functionalizations
-
Add time:08/25/2019 Source:sciencedirect.com
Use of a directing group in C–H functionalizations, often referred to as chelation assistance, is one of the most reliable methods for achieving highly efficient and highly site-selective reactions. Although a variety of transition metals can be used in directed C–H functionalization reactions, Ni-catalyzed directed C–H functionalization reactions have remained a relatively underdeveloped area of research. Recently, interest in these reactions has been renewed due to the development of a combination of a Ni catalyst and an N,N′-bidentate group; the method is now emerging as a powerful tool for Ni-catalyzed C–H functionalization reactions. However, Ni-catalyzed C–H functionalizations that do not require the use of a specific directing group (e.g., N,N′-bidentate groups) have recently been reported. Thus, Ni-catalyzed C–H functionalizations have now reached a new and interesting stage.
We also recommend Trading Suppliers and Manufacturers of 9-METHYL-7(H)-BENZO[C]CARBAZOLE (cas 117043-89-7). Pls Click Website Link as below: cas 117043-89-7 suppliers
Prev:Iridium-catalyzed silylation of unactivated C–H bonds
Next:Research paperSynthesis and photocytotoxic activity of [1,2,3]triazolo[4,5-h][1,6]naphthyridines and [1,3]oxazolo[5,4-h][1,6]naphthyridines) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis of Indazolo[2,1-a]Cinnolines via Rhodium (III)-Catalyzed C–H activation/annulation under mild conditions08/27/2019
- Research paperSynthesis and photocytotoxic activity of [1,2,3]triazolo[4,5-h][1,6]naphthyridines and [1,3]oxazolo[5,4-h][1,6]naphthyridines08/26/2019
- Iridium-catalyzed silylation of unactivated C–H bonds08/24/2019
- The synthesis, molecular structure and photophysical properties of 2, 9, 16, 23-tetrakis (7-coumarinoxy-4-methyl)-phthalocyanine sensitizer08/23/2019
- Estimation of ground and excited-state dipole moments of synthesized coumarin derivative, (S)-(1-((7-hydroxy-2-oxo-2H-chromen-4-yl)methyl)-1H-1,2,3-triazol-4-yl)methyl 2-(((9H-fluoren-9-yl)methoxy)cabonylamino)-3-phenylpropanoate from a solvatochromic shift and theoretical methods08/22/2019
- Photochemical reaction of 9-nitro-substituted anthracene-like molecules 9-methyl-10-nitroanthracene and 12-methyl-7-nitrobenz[a]anthracene☆08/21/2019


