Marzi, ElenaSchlosser, Manfred2006-03-032006-03-032006-03-03200510.1016/j.tet.2004.10.103https://infoscience.epfl.ch/handle/20.500.14299/227043WOS:0002278670000236610The organometallic approach to diversity-oriented org. synthesis was subjected to a further test, this time in the phenol series. The model compds. selected were 2,3,6-trifluorophenol, the three isomers of (trifluoromethoxy)phenol and the three isomers of chlorophenol. A combination of optionally site selective metalations and protective group-controlled metalations enabled the selective generation of several isomeric intermediates in each case and their subsequent conversion into functionalized derivs., in particular hydroxybenzoic acids. [on SciFinder (R)]Phenols Role: RCT (Reactant)RACT (Reactant or reagent) (halo; regioselective functionalization of halo-bearing phenols using a combination of optionally site selective metalations and protective group-controlled metalations); Metalation; Protective grregioselective functionalization halo phenol metalationThe site-selective functionalization of halogen-bearing phenols: an exercise in diversity-oriented organometallic synthesistext::journal::journal article::research article