Thermische Analyse Mit Biologisch Leicht Abbaubaren Hydraulik- und Getriebeölen

Different methods of thermal analysis (TG/DTG, pressure- and cooling-DSC) were used for a comparative characterization of the thermal-oxidative stabilities and low-temperature behaviour of vegetable and mineral oil-based hydraulic fluids. The mineral oil-based hydraulic fluids proved to have markedly higher thermal-oxidative stabilities than those of the vegetable oils, but they were much less biodegradable.This revised version was published online in November 2005 with corrections to the Cover Date.     

Transformation of Pectins into Non-Ionic or Anionic Surfactants Using a One-Pot and Cascade Mode Process

The present article describes the one-pot synthesis of double- and single-tailed surfactants by a cascade process that involves the hydrolysis/butanolysis of pectins into butyl galacturonate monosaccharides followed by transesterification/transacetalisation processes with fatty alcohols, and subsequent aqueous basic and acid treatments. The cascade mode allows the depolymerisation to proceed more efficiently, and the purification conditions are optimised to make the production of single-tailed surfactants more manufacturable. These products in a pure form or as mixtures with alkyl glycosides resulting from butanolysis and transglycosylation of pectin-derived hexoses, exhibit attractive surface-tension properties, especially for the n-oleyl ᴅ-galactosiduronic acid products. In addition, a readily biodegradability and an absence of aquatic ecotoxicity are shown for the galacturonic acid derivatives possessing an oleyl alkyl chain at the anomeric position.     

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

<正>As one of the most important five-member heterocyclic aromatic rings, pyrrole is widely distributed in numerous natural products and pharmaceutical agents. Asymmetric dearomatization of pyrroles is very attractive in organic synthesis given the fact that highly functionalized chira pyrrolines and pyrrolidines could be easily accessed from the readily available pyrroles. However, the reported asymmetric dearomatization reactions of pyrroles are limited to transition-metal-catalyzed [4+3] cycloaddition and hydrogenation reactions. The enantioselective intermolecular alkylative dearomatization of pyrroles is rare and challenging due to multiple selectivity issues including the