Abstract
The Meyers reaction, i.e. the nucleophilic aromatic substitution reaction between aryloxazolines with organolithium and organomagnesium reagents is a very efficient and reliable method for the formation of new carbon-carbon and carbon-heteroatom bonds. The aim of this review is to present a general overview of this reaction in chiral and racemic form, emphasizing its scope and limitations. The literature is covered since 1994.
Keywords: Nucleophilic aromatic substitution, Meyers reaction, oxazolines, Grignard reagents, organolithium reagents, nucleophilic aromatic substitution reaction, aryloxazolines, organolithium, organomagnesium reagents, carbon-heteroatom bonds, racemic form, indolines, indans, tetralins, benzofurans
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Biomass pretreatment, hydrolysis, and saccharification of carbohydrates, and sugars bioconversion in biofuels and bioproducts within a biorefinery framework. Carbohydrates derived from woody biomass, agricultural wastes, algae, sewage sludge, or any other lignocellulosic feedstock are included in this issue. Simulation, techno-economic analysis, and life cycle analysis of a biorefinery process are ...read more
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