An article Halogen-Lithium Exchange of Sensitive (Hetero)aromatic Halides under Barbier Conditions in a Continuous Flow Set-Up WOS:000565246900002 published article about ORGANOLITHIUM COMPOUNDS; KETONES; LITHIATION; CHEMISTRY; ARYLATION; REAGENTS; CATALYST; AMIDES; ACIDS in [Weidmann, Niels; Harenberg, Johannes H.; Knochel, Paul] Ludwig Maximilians Univ Munchen, Dept Chem, Butenandtstr 5-13, D-81377 Munich, Germany; [Nishimura, Rodolfo H., V] Univ Fed Vale Sao Francisco, Colegiado Ciencias Farmaceut, Ave Jose de Sa Manicoba, BR-56304205 Petrolina, Petrolina, Brazil in 2021, Cited 57. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Recommanded Product: 4-Methoxybenzaldehyde
A halogen-lithium exchange reaction of (hetero)aromatic halides performed in the presence of various electrophiles such as aldehydes, ketones, Weinreb amides, and imines using BuLi as exchange reagent and a commercially available flow set-up is reported. The organolithiums generated in situ were instantaneously trapped with various electrophiles (Barbier conditions) resulting in the formation of polyfunctional (hetero)arenes. This method enables the functionalization of (hetero)arenes containing highly sensitive functional groups such as esters, which are not tolerated in batch conditions.
Recommanded Product: 4-Methoxybenzaldehyde. Welcome to talk about 123-11-5, If you have any questions, you can contact Weidmann, N; Nishimura, RHV; Harenberg, JH; Knochel, P or send Email.
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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