An asymmetric cyclization of alkynols triggered addition of azlactones catalyzed by a combined catalyst system consisting of a chiral gold phosphate and a phosphoric acid produces conformationally restricted amino acid precursors bearing vicinal quaternary stereogenic centers in high levels of stereoselectivity. 2011 Elsevier Ltd. All rights reserved. The enantioselective construction of quater...

Temperature-dependent magnetic second-harmonic generation (MSHG) at normal incidence (NI) is used to determine magnetization curves from Au-capped ultrathin Fe nanostructures grown on a vicinal W(110) substrate. Aligned magnetic nanostructures grown on low-symmetry interfaces are generally inhomogeneous, with different magnetic species, such as terrace and step atoms, contributing to the overal...

The synthesis of a series of α-trifluoromethylcyclohexanols and analogous trimethylsilyl ethers by addition of the Ruppert-Prakash reagent to substituted cyclohexanones is presented. A method for the assignment of configuration of such compounds, of related α-trifluoromethylcyclohexylamines and of quaternary trifluoromethyl-substituted carbons is described based on the determination of the (3)J...

21 vanadium bis-phenolate benzimidazolyidene complexes spanning three oxidation states have been investigated. Special emphasis is thereby laid on their salt metathesis reactivity and the accessibility of +IV state by reductive or oxidative routes, starting from vanadium(V) vanadium(III) respectively. While route highly depended reducing agent material used, gives clean access to vanadium(IV) d...

Background: Enantiopure epoxides are important intermediates in the synthesis of high-value chiral chemicals. Epoxide hydrolases have been exploited in biocatalysis for kinetic resolution of racemic epoxides to produce enantiopure epoxides and vicinal diols. It is necessary to obtain sufficient stable epoxide hydrolases with high enantioselectivity to meet the requirements of i...