Category: pyridine-derivatives. Authors Lima, F; Meisenbach, M; Schenkel, B; Sedelmeier, J in ROYAL SOC CHEMISTRY published article about in [Lima, Fabio] Novartis Pharma AG, Novartis Inst Biomed Res, Global Discovery Chem, Basel, Switzerland; [Lima, Fabio; Meisenbach, Mark; Schenkel, Berthold; Sedelmeier, Joerg] Novartis Pharma AG, Chem & Analyt Dev, Basel, Switzerland; [Sedelmeier, Joerg] F Hoffmann La Roche Ltd, Small Mol Tech Dev, Basel, Switzerland in 2021, Cited 46. The Name is Ethyl nicotinate. Through research, I have a further understanding and discovery of 614-18-6
We herein report two complementary strategies employing organolithium chemistry for the synthesis of glyoxal derivatives. Micro-mixer technology allows for the generation of unstable organometallic intermediates and their instantaneous in-line quenching with esters as electrophiles. Selective mono-addition was observed via putative stabilized tetrahedral intermediates. Advantages offered by flow chemistry technologies facilitate direct and efficient access to masked 1,2-dicarbonyl compounds while mitigating undesired by-product formation. These two approaches enable the production of advanced and valuable synthetic building blocks for heterocyclic chemistry with throughputs of grams per minute.
About Ethyl nicotinate, If you have any questions, you can contact Lima, F; Meisenbach, M; Schenkel, B; Sedelmeier, J or concate me.. Product Details of 614-18-6
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem