On July 14, 2020, Ouyang, Lu; Xia, YanPing; Wei, YiFei; Liao, Jianhua; Luo, Renshi published an article.Product Details of 79815-20-6 The title of the article was Highly Catalytic Enantioselective Reformatsky Reaction with Aldehydes and Ketones Using an Available Prolinol Ligand. And the article contained the following:
A highly Me2Zn-mediated catalytic enantioselective Reformatsky reaction of aldehydes and ketones with Et iodoacetate using a readily available prolinol ligand is reported. This reaction provides an efficient method for the construction of β-hydroxy esters in up to 98% yield and 95% enantiomeric excess (ee) value. A wide range of functional groups are tolerated and the practicality of this protocol is demonstrated by performing the reaction on a gram scale. The experimental process involved the reaction of H-Idc-OH(cas: 79815-20-6).Product Details of 79815-20-6
The Article related to enantioselective reformatsky reaction aldehyde ketone iodoacetate prolinol ligand, hydroxy ester enantioselective synthesis, General Organic Chemistry: Synthetic Methods and other aspects.Product Details of 79815-20-6
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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