Ester Formation via Nickel-Catalyzed Reductive Coupling of Alkyl Halides with Chloroformates was written by Zheng, Min;Xue, Weichao;Xue, Teng;Gong, Hegui. And the article was included in Organic Letters in 2016.SDS of cas: 1841512-58-0 This article mentions the following:
The synthesis of alkyl esters from readily available alkyl halides and chloroformates was achieved for the first time using a mild Ni-catalyzed reductive coupling protocol. Unactivated primary and secondary alkyl iodides as well as glycosyl, benzyl, and aminomethyl halides were successfully employed to yield products in moderate to excellent yields with high functional group tolerance. In the experiment, the researchers used many compounds, for example, 1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate (cas: 1841512-58-0SDS of cas: 1841512-58-0).
1,3-Dioxoisoindolin-2-yl 4-phenylbutanoate (cas: 1841512-58-0) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.SDS of cas: 1841512-58-0
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Indole alkaloid derivatives as building blocks of natural products from聽Bacillus thuringiensis聽and聽Bacillus velezensis聽and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles