Regioselective synthesis of functionalized salicylates, isotetronic acids, and alkylidene-isobenzofurans based on one-pot cyclizations of silyl enol ethers Dede, Rüdiger , 1977- Text theses Text Hochschulschrift 2008 2008 eng electronic resourceremoteComputermedienOnline-RessourceOnline-Ressource graph. Darst. This work is a contribution to the chemistry of different types of silyl enol ethers which were applied to the regioselective synthesis of functionalized salicylates, isotetronic acids, and alkylidene-isobenzofurans. In addition, the competition between the recently developed domino Staudinger / semi-aza-Wittig / fragmentationʺ reaction of γ-azido-ß-hydroxyketones and the normal aza-Wittig reaction pathway was studied. Rüdiger Dede Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2008 540 35.69 http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2008-0067-5 http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2008-0067-5&pdf http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2008-0067-5 Regioselective synthesis of functionalized salicylates, isotetronic acids, and alkylidene-isobenzofurans based on one-pot cyclizations of silyl enol ethers--(DE-627)572573855 urn:nbn:de:gbv:28-diss2008-0067-5 oclc: 277047845 ppn: (DE-627)576755303