Visible-Light-Promoted Carbene Insertion and Decarbonylation for the Synthesis of α-Substituted γ-Ketoesters was written by Li, Weina;Yang, Yingying;Tang, Zhiliang;Yu, Xianglin;Lin, Jun;Jin, Yi. And the article was included in Journal of Organic Chemistry in 2022.Related Products of 584-74-7 This article mentions the following:
Herein, a blue visible-light-promoted approach to prepare a variety of α-substituted γ-ketoesters derivatives RC(O)CH2C(COOR1)R2R3 [R = Ph, 3-FC6H4, 4-MeC6H4, etc.; R1 = Me, Et; R2 = H, CHO; R3 = Ph, 4-ClC6H4, 3-thienyl, etc.] through carbene insertion and the decarbonylation of enaminones and diazoesters was reported. These reactions used readily available starting materials, as well as transition-metal-free, eco-friendly procedures that were amenable to gram-scale synthesis and wide functional group tolerance. This methodol. might be useful for constructing polysubstituted heterocycles with potential biol. activity. In the experiment, the researchers used many compounds, for example, Ethyl 2-fluorophenylacetate (cas: 584-74-7Related Products of 584-74-7).
Ethyl 2-fluorophenylacetate (cas: 584-74-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Related Products of 584-74-7
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics