33236-96-3Relevant articles and documents
A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane
Khamarui, Saikat,Sarkar, Deblina,Pandit, Palash,Maiti, Dilip K.
supporting information; experimental part, p. 12667 - 12669 (2012/01/03)
A general strategy for fast decarboxylative difunctionalization to gem-dihalohydrin, gem-dihaloether, gem-dibromoester and cyclized bromo-1,4-dioxane synthons with outstanding regio- and stereoselectivity is demonstrated. The Royal Society of Chemistry 20
Substituent Dependence of the Selectivity in Alkene Bromination through Bromocarbenium Ions
Bienvenue-Goetz, Elizabeth,Dubois, Jaques-Emile
, p. 5388 - 5392 (2007/10/02)
Substituent effects on the rates of bromination of alkenes GαRαC=CRβR'β, where G is a conjugatively electron-donating group, are consistent with a carbenium ion like transition state, whereas by the same criteria the transition state for nonconjugated alkenes is bromonium type.The reactivities of compounds with the same substituent G are analyzed in terms of the sensitivity to structural and solvent effects.The lowest sensitivity is attributed to the earliest transition state.The dependence of the reaction constant on G leads to a general equation including cross terms: log k = -7.7Σ(?p+)α - 13.7Σ(?m+)β - 7.0(?p+)Gα(?p+)Rα - 5.8Σ(?p+)αΣ(?m+)β + 1.64.The carbenium ion character, common to both bromination and hydration, results in highly dissymmetric α- and β-substituent effects.However, these two reactions respond differently to β-substituents: a β methyl increases the bromination rate but decreases the hydration rate.Similarities and differences in the transition state models are discussed; the kinetic data suggest that the transition state is earlier in bromination than in hydration.
