16878-48-1Relevant articles and documents
Structure-reactivity relationships and intrinsic reaction barriers for nucleophile additions to a quinone methide: A strongly resonance-stabilized carbocation
Richard, John P.,Toteva, Maria M.,Crugeiras, Juan
, p. 1664 - 1674 (2000)
Second-order rate constants k(Nu) (M-1 s-1) were determined for addition of a wide range of nucleophiles to the simple quinone methide 4- [bis(trifluoromethyl)methylene]cyclohexa-2,5-dienone (1) to give the nucleophile adduct 1-Nu in
Mechanisms for the Uncatalyzed and Hydrogen Ion Catalyzed Reactions of a Simple Quinone Methide with Solvent and Halide Ions
Richard, John P.
, p. 4588 - 4595 (2007/10/02)
The quinone methide 4-[bis(trifluoromethyl)methylene]cyclohexa-2,5-dienone (1) has been prepared in situ from the solvolysis of 4-MeOArC(CF3)2OTs in 50:50 (v/v) trifluoroethanol/water, and its reactions with solvent and halide ions h