In 2022,Tang, Zhishun; Chen, Linghong; Yin, Pengxuan; Yang, Lu; Shi, Zhichuan; Zhao, Zhigang; Ye, Ling; Li, Xuefeng published an article in Organic & Biomolecular Chemistry. The title of the article was 《Diastereoselective construction of tetracyclic chromanes via a triply annulative strategy》.Recommanded Product: 623-47-2 The author mentioned the following in the article:
A triple Michael/aldol cascade reaction was established to construct tetracyclic chromanes in a diastereoselective fashion (≥5 : 1 dr). The polycyclic products were generated in 50-78% isolated yields under mild and metal-free conditions. Five reactive sites of enolate-tethered divinyl ketones were sequentially utilized to form four C-C bonds in a one-pot operation, leading to a construction of three new rings. Up to six consecutive stereocenters, including two quaternary stereogenic centers, were created in this domino process.Ethyl propiolate(cas: 623-47-2Recommanded Product: 623-47-2) was used in this study.
Ethyl propiolate(cas: 623-47-2) is a clear colorless to pale yellow liquid that is soluble in ethanol, ether and chloroform. It an important organic chemical raw material and pharmaceutical intermediate. Ethyl propargylate is obtained by oxidation of propargyl alcohol to propargylic acid followed by esterification.Recommanded Product: 623-47-2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics