129103-70-4Relevant academic research and scientific papers
Kinetic study of hydrolysis of benzoates. Part XXIV-variation of the ortho substituent effect with solvent in the alkaline hydrolysis of substituted phenyl benzoates
Nummert, Vilve,Piirsalu, Mare,Maeemets, Vahur,Koppel, Ilmar
, p. 1138 - 1144 (2005)
The second-order rate constants k2 (M-1 s -1 ) for the alkaline hydrolysis of meta-, para- and orthosubstituted phenyl benzoates, C6H5CO 2C6H4X, in aqueous 0.5 M n-Bu4NBr were measured spectrophotometrically. The dependence of substituent effects, especially ortho inductive, resonance and steric terms on different solvent parameters, was studied using the following equation: Δ log k ortho = c0 + c1(ortho) σ1 + c2(ortho) σR0 + c 3(ortho)EsB + c4ΔE + c 5ΔY + c6ΔP + c7(ortho) ΔEσI + c8(ortho)ΔYσI + c9(ortho) ΔPσI + c10(ortho) ΔEσR0 + c11(ortho) ΔYσR0 + c12(ortho) ΔPσR0 where Δlog k = log kX - log KH, σI, σR0 and E SB are the inductive, resonance and steric substituent constants and E, Y and P are the solvent electrophilicity, polarity and polarizability parameters, respectively. In data treatment ΔE = E s - EH2O, ΔY = YS -YH2O and ΔP = PS - PH2O were used. The solvent electrophilicity was found to be the main factor responsible for changes in the ortho, para and meta polar substituent effects with medium. The variation of the ortho inductive term with the solvent electrophilicity ES was found to be ca threefold smaller than that for para substituents, whereas the ortho resonance term appeared to vary with solvent very similarly to that for para substituents. The steric term of ortho substituents was found to be approximately independent of solvent parameters. The ortho effect caused by the supplementary inductive effect from ortho position was found to disappear in a solvent whose electrophilic solvating power is comparable to that of 60% aqueous ethanol (E ≈ 13.3). Copyright
Synthesis of benzoate-functionalized phosphanes as novel building blocks for the traceless staudinger ligation
Mamat, Constantin,Flemming, Anke,Koeckerling, Martin,Steinbach, Joerg,Wuest, Frank R.
experimental part, p. 3311 - 3321 (2010/03/03)
A new synthetic pathway for the preparation of benzoate-functionalized phosphanes for microwave-mediated traceless Staudinger ligations is described. Novel phosphane derivatives based on 4-substituted iodophenyl benzoates were prepared via palladium(II)-catalyzed P-C cross-coupling reaction strategy in high yields. The application of microwave conditions for the ligation reactions reduced the reaction time considerably. An approach to fast and facile labeling strategies using this ligation was established.
Synthesis of 3-Acyl- and 3-Carbamoylflavones
Ellemose, Steen,Kure, Niels,Torsell, Kurt B. G.
, p. 524 - 529 (2007/10/02)
Routes to 3-acyl-, 3-carboxamido- and polyhydroxylated flavones have been devised by application of isoxazole methodology and Heck-Stille couplings.Reductive ring opening of 3-alkoxyisoxazoles gives β-keto carboxamides in contrast with 3-alkoxy-2-isoxazolines, which give β-hydroxy esters.
A Complex Induced Proximity Effect in the Anionic Fries Rearrangement of o-Iodophenyl Benzoates: Synthesis of Dihydro-O-methylsterigmatocystin and Other Xanthones
Horne, Stephen,Rodrigo, Russell
, p. 4520 - 4522 (2007/10/02)
The success of an anionic Fries rearrangement, used to synthesise dihydro-O-methylsterigmatocystin and other xanthones, is dependent on the presence of a remote methoxyl substituent.
