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Electrophilic Thiocyanato Reagent Assisted Oxa-Michael/Thiocyanation of α,β-Unsaturated Ketones. | LitMetric

Electrophilic Thiocyanato Reagent Assisted Oxa-Michael/Thiocyanation of α,β-Unsaturated Ketones.

J Org Chem

School of Chemistry & Chemical Engineering, Beijing Institute of Technology (Liangxiang Campus), No. 8 Liangxiang East Road, Fangshan District, Beijing 102488, China.

Published: December 2021

A route for thiocyanation-functionalization of the electron-deficient C═C double bond was developed. Regioselective thiocyanation-etherification of α,β-unsaturated ketones was achieved. The desired products were obtained in moderate to high yields under mild conditions. It was suggested that the nucleophile was activated by the electrophilic thiocyanato reagent, and difunctionalization was achieved through a 1,4-addition/thiocyanation pathway.

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Source
http://dx.doi.org/10.1021/acs.joc.1c01993DOI Listing

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