Isolation of Bisphenol A-Tolerating/degrading Shewanella haliotis Strain MH137742 from an Estuarine Environment

Applied Biochemistry and Biotechnology - The human exposure to bisphenol A (BPA) occurs frequently. Once, this compound was one of the highest volume chemicals produced worldwide and used as a...     

The liquid-crystalline properties of bis[N-[[4-[4-(alkoxy)benzoyloxy]2-hydroxyphenyl]methylene]alkanamino] complexes of Cu(II), Pd(II) and Ni(II). A general view

The thermotropic liquid-crystalline phase behaviour of a homologous set of bis[N-[[4-[4-(alkoxy)benzoyloxy]2-hydroxyphenyl]methylene]alkanamino] copper(II) complexes is examined. New data are reported and taken into account in addition to those previously reported in this Journal. The influence of alkoxy and alkanamine groups on the nature and stability of the mesophase is underlined. As a general trend, with some notable exception, smectic (C type) mesomorphism is favoured by longer alkoxy and alkanamine chains. Data concerning some Pd(II) and Ni(II) homologous complexes are also reported. The mesophase stability (nematic phase) is higher for palladium and nickel complexes than for the copper containing homologues.     

A highly active fungal β-glucosidase

A highly active thermostable β-glucosidase was purified to homogeneity from a strain ofTrichoderma sp. The enzyme was an extracellular glycoprotein and showed hydrolytic activity toward several β-glucosides. Cellobiose was found to be the substrate of choice for this enzyme. This finding could suggest future technological applications of the purified protein.     

On nash theory of Arc structure of singularities

Sunto Si ha l'intenzione d'incominciare lo studio sistematico della teoria abbozzata da John Nash circa venticinque anni fa, dove si associa a una varietà algebrica singolare X spazi i cui ponti corrispondono genericamente a troncature di certi rami analitici parametrizati su X. In questo articolo si presentano accuratamente i fondamenti della teoria. Inoltre, con questi metodi (e nozioni della teoria della equisingolarità per le curve sghembe) s'introducono nuovi invarianti di una singolarità, si spera di studiarli più accuratamente in futuri lavori.     

Crystal and molecular structure of thiamine monochloride

The crystal and molecular structure of thiamine monochloride (C₁₂H₁₇N₄OSCl) was determined by X-ray diffraction and refined to a finalR value of 0.042. The compound crystallizes in the monoclinic system, space groupP2₁/a, with cell constantsa=18.929(4),b=11.663(2),c=6.376(2) Å and=96.72(8)°. The thiamine molecule is anhydrous and unprotonated, and the torsion angles at the methylene carbon show that it possesses anF conformation. The dihedral angle value of 84.16(6)° between thiazolium and pyrimidine rings is in the normal range found for the thiamine withF conformation, protonated or not, hydrated or not. Thiamine therefore has the same conformation notwithstanding protonation or hydration, with the rings similarly oriented in all the crystal structures containing thiamine.     

DARK EXCITATION OF CHLOROPHYLL

Abstract— Enzyme generated triplet acetone transfers its energy to Chl a to form the first excited singlet of the acceptor, as shown by the suppression of the acetone chemiphosphorescence and concomitant appearance of the Chl fluorescence.     

Hetarylpyrazoles. II. Reactions of pyrazol-l'-ylpyridines

Pyrazol-l'-ylpyridines undergo electrophilic substitution reactions (bromination, chlorination, and nitration) preferentially in the pyrazole ring. There is some evidence of the mutual influence of the pyrazole and the pyridine ring on the reactivity of the system. Some modifications of the substituents were also carried out. A dihydro derivative of a new ring system, pyrazolo[1′,2′-a]pyrido[2,1-c][l,2,4]triazine was also obtained.     

Intramolecular silyl migration in the singlet oxygenation of 2-methyl-5-trimethylsilylfuran

Tetraphenylporphyrin-sensitized photooxygenation of 2-methyl-5-trimethylsilylfuran ($\text{4}$) affords quantitatively trimethylsilyl 2-oxo-4-pentenoate ($\text{5}$), presumably via intramolecular Baeyer-Villiger rearrangement of the intermediary dioxirane ($\text{3a}$).     

Diastereoselective synthesis of cularine alkaloids via enium ions and an easy entry to isoquinolines by aza-Wittig electrocyclic ring closure

In preliminary communications, we reported the diastereoselective synthesis of cularine and sarcocapnine via the intramolecular ring closure of nitrenium and oxenium ions, a new highly diastereoselective reductive methylation with (+)-8-phenylmenthyl chloroacetate followed by reduction with sodium borohydride, and a facile entry to the isoquinoline precursors by aza-Wittig electrocyclic ring closure. We now report the full details of the syntheses of (+)-O-demethylcularine, (+)-cularine, (+)-sarcocapnidine, (+)-sarcocapnine, and (+)-crassifoline and describe different methods of synthesis of their precursors.