An article Divergent Total Syntheses of Yaequinolone-Related Natural Products by Late-Stage C-H Olefination WOS:000649101400020 published article about INSECTICIDAL ANTIBIOTICS; PENICILLIUM SP; ASPERGILLUS-NIDULANS; ALKALOIDS; DERIVATIVES; MARINE in [Jia, Wen-Liang; Ces, Sabela Vega; Fernandez-Ibanez, M. Angeles] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1098 XH Amsterdam, Netherlands in 2021.0, Cited 41.0. Application In Synthesis of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
Divergent total syntheses of 10 yaequinolone-related natural products have been achieved for the first time by latestage C-H olefination of 3,4-dioxygenated 4-aryl-5-hydroxyquinolin-2(1H)-ones, core structures of this family of natural products. A robust synthetic methodology to construct the core structures has been established, and the C-H olefination reaction has been carried out with synthetically useful yields and high levels of site-selectivity under mild reaction conditions in the presence of a Pd/S,O-ligand catalyst.
Application In Synthesis of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Jia, WL; Ces, SV; Fernandez-Ibanez, MA or concate me.
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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