Synthesis of 3-aryl-3,4-Dihydroisocoumarins and sterically encumbered Biaryls by [3+3] Cyclocondensation Reactions and synthesis of Functionalized Fluoranthenes, trifluoromethyl-Substituted Di- and Terphenyls and tetraaryl-p-Benzoquinones by Pd(0)-Catalysed Cross-Coupling Reactions

10.18453/rosdok_id00000953 Ullah, Ihsan Ihsan Ullah http://d-nb.info/gnd/1020214473 Synthesis of 3-aryl-3,4-Dihydroisocoumarins and sterically encumbered Biaryls by [3+3] Cyclocondensation Reactions and synthesis of Functionalized Fluoranthenes, trifluoromethyl-Substituted Di- and Terphenyls and tetraaryl-p-Benzoquinones by Pd(0)-Catalysed Cross-Coupling Reactions Universität Rostock 2011 540 Chemistry & allied sciences 2011 en http://purl.uni-rostock.de/rosdok/id00000953 urn:nbn:de:gbv:28-diss2011-0189-5 Salicylates, 3-aryl-3,4-dihydroisocoumarins and sterically encumbered and functionalized biaryls were synthesized using 1,3-bis(silyl enol ethers) by TiCl4-mediated regioselective [3+3] cyclocondensation strategy. While functionalized fluoranthenes, 4-aryl-1-bromo-2-trifluoromethylbenzenes, 2,5-diaryl-1-trifluoromethylbenzene and terphenyls and tetraaryl-p-benzoquinones were synthesized by palladium(0)-catalyzed Heck and Suzuki cross coupling reactions.