COA of Formula: C7H6O2. In 2019.0 J ORG CHEM published article about PRACTICAL SYNTHESIS; ORGANIC-SYNTHESIS; PROTEIN-KINASE; POTENT; LOK; 2,4(5)-DIARYL-1H-IMIDAZOLES; 2,4(5)-DIARYLIMIDAZOLES; 4(5)-ARYL-1H-IMIDAZOLES; ARYLATION in [de Toledo, Ian; Grigolo, Thiago; Pilli, Ronaldo A.] Univ Estadual Campinas, Inst Chem, Dept Organ Chem, UNICAMP, BR-13083970 Campinas, SP, Brazil; [Bennett, James M.; Elkins, Jonathan M.] Univ Oxford, Nuffield Dept Med, Struct Genom Consortium, Old Rd Campus Res Bldg,Roosevelt Dr, Oxford OX3 7DQ, England; [Elkins, Jonathan M.] Univ Estadual Campinas, Dept Genet & Evolucao, Inst Biol, Struct Genom Consortium, BR-13083886 Campinas, SP, Brazil in 2019.0, Cited 40.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.
A one-pot and modular approach to the synthesis of 2,4(5)-disubstituted imidazoles was developed based on ketone oxidation, employing catalytic HBr and DMSO, followed by imidazole condensation with aldehydes. This methodology afforded twenty-nine disubstituted NH-imidazoles (23%-85% yield). A three-step synthesis of 20 kinase inhibitors was achieved by employing this oxidation- condensation protocol, followed by bromination and Suzuki coupling in the imidazole ring to yield trisubstituted NH-imidazoles (23%-69%, three steps). This approach was also employed in the synthesis of known inhibitor GSK3037619A.
COA of Formula: C7H6O2. Welcome to talk about 100-83-4, If you have any questions, you can contact de Toledo, I; Grigolo, T; Bennett, JM; Elkins, JM; Pilli, RA or send Email.
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