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- W4210958219 endingPage "337" @default.
- W4210958219 startingPage "303" @default.
- W4210958219 abstract "An allylic substitution has been accomplished by allowing two different substrate catalyst complexes to react together in a “dual catalytic” system. The reaction occurs after the allyl carbonate is converted into a substratepalladium metal catalyst complex and reacted with a vanadium metal–propargyl alcohol catalyst complex, giving the allylic substitution product. This chapter discusses four reviews on allylic substitution reactions. It also deals with reviews on oxirane ring-opening reactions. The chapter focuses on the use of ionic liquids in SN2 reactions. Density functional theory (DFT) calculations determine the rates of formation of aminofunctionalized ionic liquids in the SN2 reaction between various N-substituted imidazoles and 2-bromoethylamine. The chapter reviews the use of Brønsted acids, Lewis acids, metal complexes, and heteropoly acids as catalysts in the conversion of alcohols to carbenium ions in SN1 reactions." @default.
- W4210958219 created "2022-02-13" @default.
- W4210958219 creator A5049645853 @default.
- W4210958219 date "2014-04-04" @default.
- W4210958219 modified "2023-09-23" @default.
- W4210958219 title "Nucleophilic Aliphatic Substitution" @default.
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