Rhodium(I)-Catalyzed Coupling-Cyclization of C=O Bonds with α-Diazoketones was written by Chen, Ziyang;Hu, Xinwei;Huang, Junmin;Zeng, Wei. And the article was included in Organic Letters in 2018.Formula: C12H14O3 This article mentions the following:
An unprecedented intermol. nucleophilic attack of C=X bonds (X = O and S) on the rhodium(I)-carbenes has been developed. This transformation allows for the coupling-cyclization of aroylamides with α-diazoketones and provides concise access to 2,4,5-trisubstituted 1,3-oxazoles, e.g., I, and 1,3-thiazoles, e.g., II, with a broad tolerance of functional groups. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9Formula: C12H14O3).
Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Formula: C12H14O3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics