Recommanded Product: 123-11-5. Wagner, CJ; Salisbury, EA; Schoonover, EJ; VanderRoest, JP; Johnson, JB in [Wagner, Cole J.; Salisbury, Eric A.; Schoonover, Erik J.; VanderRoest, Jacob P.; Johnson, Jeffrey B.] Hope Coll, Dept Chem, 35 East 12th St, Holland, MI 49423 USA published Pyridine-directed carbon-carbon single bond activation: Rhodium-catalyzed decarbonylation of aryl and heteroaromatic ketones in 2021.0, Cited 50.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.
The decarbonylation of 2-pyridyl-substituted ketones via transition metal-catalyzed carbon-carbon bond activation provides ready access to a variety of biaryl compounds. The highly efficient and general method provides reliable decarbonylation of benzophenones including a range of functional groups and substitution patterns. The methodology has also proven highly efficient for heteroaromatic substrates, including those containing thiophenyl, indolyl, quinolinyl, and pyridine substitution. (C) 2021 Elsevier Ltd. All rights reserved.
Recommanded Product: 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Wagner, CJ; Salisbury, EA; Schoonover, EJ; VanderRoest, JP; Johnson, JB or concate me.
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