29584-99-4Relevant articles and documents
Fast oxidation of secondary alcohols by the bromate-bromide system using cyclic microwave heating in acidic water
P??kk?nen, Sanna,Pursiainen, Jouni,Lajunen, Marja
, p. 6695 - 6699 (2010)
We report an improved, gentle, cyclic microwave activation technique for the oxidation of secondary alcohols using nonhazardous hypobromous acid (BrOH) as the reagent in acidic water. Several aliphatic and aromatic secondary alcohols were successfully oxidized to the corresponding ketones using this technique in high yields and with only minor amounts of side products.
Experimental and theoretical studies on the reactivities of partially and fully fluorinated primary alkyl radicals
Bartberger, Michael D.,Dolbier Jr., William R.,Lusztyk,Ingold
, p. 9857 - 9880 (2007/10/03)
Absolute rate constants for hydrogen abstraction from n-Bu3SnH by a number of partially-fluorinated and fully fluorinated n-alkyl radicals have been measured. The C-H and C-C bond dissociation energies for a number of pertinent hydrofluorocarbons have been calculated by DFT. The rate data are compared with those for addition of the same radicals to styrene, and the reactivities of these radicals are discussed in terms of their electronegativies, their structure and the thermodynamics of their reactions.