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Catalyst and Additive‐Free Selective Ring‐Opening Selenocyanation of Heterocycles with Elemental Selenium and TMSCN

Liguo Lu, Kang Bi, Xiaobo Huang, Miaochang Liu, Yunbing Zhou, Huayue Wu

2021Advanced Synthesis & Catalysis22 citationsDOI

Abstract

Abstract A catalyst and additive‐free strategy for selective ring‐opening selenocyanation of saturated heterocycles with elemental selenium and TMSCN is developed, affording a series of aliphatic selenocyanates and selenaheterocycles. In the case of unprotected unstrained N‐heterocycles, the reactions offer ammonium selenonitriles that prove to be an efficient selenonitrile reagent. magnified image

Topics & Concepts

ChemistryReagentSeleniumRing (chemistry)CatalysisOrganic chemistryElemental analysisAmmoniumCombinatorial chemistryOrganoselenium and organotellurium chemistrySulfur-Based Synthesis TechniquesCatalytic C–H Functionalization Methods
Catalyst and Additive‐Free Selective Ring‐Opening Selenocyanation of Heterocycles with Elemental Selenium and TMSCN | Litcius