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Bond energy enabled amine distinguishing strategy: chemo-, regioselective 1,3-diamination of (trifluoromethyl)alkenes with different amines by two C(sp<sup>3</sup>)–F bond cleavages

Hao Zeng, Hengyuan Li, Chengxi Li, Huanfeng Jiang, Chuanle Zhu

2022Organic Chemistry Frontiers21 citationsDOI

Abstract

ipso -Defluorinative amination-triggered 1,3-diamination of (trifluoromethyl)alkenes with different amines affords various monofluoroalkenylated acyclic 1,3-diamines in high yields with excellent Z / E selectivity.

Topics & Concepts

ChemistryAminationTrifluoromethylRegioselectivityAmine gas treatingSelectivityMedicinal chemistryOrganic chemistryCombinatorial chemistryCatalysisAlkylFluorine in Organic ChemistryCatalytic C–H Functionalization MethodsSynthesis and Catalytic Reactions
Bond energy enabled amine distinguishing strategy: chemo-, regioselective 1,3-diamination of (trifluoromethyl)alkenes with different amines by two C(sp<sup>3</sup>)–F bond cleavages | Litcius