%0 Book
%T Synthesis of functionalized triarylmethanes based on cyclocondensations of 1,3-Bis(silyloxy)-1,3-butadienes, one-pot synthesis of functionalized pyranones and synthesis of functionalized indoles and pyrroles based on Pd(0)-catalyzed reactions
%A Ahmad, Rasheed
%D 2009
%G English
%F 608456802
%O vorgelegt von Rasheed Ahmad
%O Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2009
%X Dianions and masked dianions represent important building blocks for the regioselective formation of carbon-carbon bonds. Cyclocondensation reactions of 1,3-bis(silyl enol ethers) with different mono(silyl enol ethers) provide an elegant approach for the synthesis of various complex carba-cycles from simple starting materials. A variety of functionalized and sterically encumbered triarylmethanes are prepared by combination of FeCl3-catalyzed benzylations of 1,3-diketones and formal [3+3] cyclocondensation reactions of mashed dianions. In this context, 4-methoxy-, 4-chloro and 4-fluoro-substituted triarylmethanes are prepared. Furthermore, dianions were converted to pyranones by reaction with functionalized benzaldehydes. Various pyranones were synthesized containing 3-bromo-, 4-methyl-, 4-phenyl-, 4-methoxy- and 4-hydoxy-substituted phenyl groups.
%L 540
%9 theses
%9 Text
%9 Hochschulschrift
%U http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2009-0150-8
%U http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2009-0150-8&pdf
%U http://rosdok.uni-rostock.de/file/rosdok_derivate_000000003973/Dissertation_Ahmad_2009.pdf
%U http://d-nb.info/997079835/34
%U http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2009-0150-8