A novel class of azatricyclononanes: pentasubstituted cyclopropanes from an uncatalysed reaction

The direct and versatile stereoselective synthesis of a novel class of cyclopropyl derivatives of pyroglutamic acid is reported, using substituted diaryldiazo compounds. The course of the reaction has been investigated, and yields of substituted fluorenylcyclopropanes are greater than those of diphenylmethylcyclopropane analogues.     

Pursuit of optimal carbohydrate-based anticancer vaccines: preparation of a multiantigenic unimolecular glycopeptide containing the Tn, MBr1, and Lewis(y) antigens.

A novel preparation of nonnatural glycoamino acids starting from n-pentenyl glycosides is described. The approach involves a Horner-Emmons olefination with a suitably protected glycine-derived phosphonate, followed by catalytic asymmetric hydrogenation, which proceeds with excellent diastereomeric selectivity. The synthetic methodology was useful for the preparation of glycoamino acids containing the Tn antigen, the MBr1 antigen (Globo-H), the Le(y) antigen, and lactose. These glycoamino acids can also serve as units for peptide synthesis. The synthesis of polyvalent glycopeptides containing three different antitumor antigens is described (28 and 29), and these have been prepared for conjugation to carrier protein in order to access the immunogenicity for tumor immunotherapy applications.     

207Pb N.M.R. of lead(II) soaps in solid,liquid-crystalline and liquid phases

Abstract

²⁰⁷Pb N.M.R. data are reported for a number of even chain length lead(II) carboxylates (soaps) at various temperatures. At room temperature, the solid lead(II) decanoate and tetradecanoate show similar spectra, with a single metal ion site, and modest shielding anisotropy. As the temperature is increased, the soaps (hexanoate to octadecanoate) all form a highly ordered smectic phase, which gives a very broad ²⁰⁷Pb signal of linewidth comparable to that of the solid phase. At higher temperatures, the hexanoate to dodecanoate soaps form a lamellar L _α (smectic A) phase, whilst the longer chain length carboxylates melt directly to the liquid phase. Both the lamellar L _α and liquid phase give fairly sharp, isotropic signals, whose chemical shifts and linewidths are strongly temperature dependent. Possible explanations for this effect include paramagnetic contributions to the shielding tensor from low-lying electronic states of Pb(II), and contributions to the observed signal from different coordination species produced in the lead(II) carboxylate system. Although there are discrete changes in chemical shift at the phase transition, the magnitudes observed in all the phases are similar, suggesting that there are no dramatic changes in the metal coordination environment.     

Die Prote?ne der Erbse

Ohne ZusammenfassungNach dem Journal of Biological Chemistry Vol. III, Juli 1907, bearbeitet und übersetzt von Dr. V. Griessmayer.     

Textilien

Ohne Zusammenfassung     

Crossed products of operator systems

In this paper we introduce the crossed product construction for a discrete group action on an operator system. In analogy to the work of E. Katsoulis and C. Ramsey, we describe three canonical crossed products arising from such a dynamical system. We describe how these crossed product constructions behave under G-equivariant maps, tensor products, and the canonical $C^{?}$-covers. We show that hyperrigidity is preserved under two of the three crossed products. Finally, using A. Kavruk's notion of an operator system that detects $C^{?}$-nuclearity, we give a negative answer to a question on operator algebra crossed products posed by Katsoulis and Ramsey.     

Silicon-29 NMR study of the formation of monomethoxysilicic acid in methanolic alkaline silicate solutions

Silicon-29 NMR spectra were obtained for more than 20 aqueous alkaline silicate solutions containing methanol. A signal assigned to CH₃OSi(OH)₃ or one of its deprotonated congeners was studied in detail for the first time for the solution conditions involved. Its appearance was monitored as a function of the solution compositions. The pseudo-equilibrium constant for its formation is of the order of 0.65. Copyright © 2001 John Wiley & Sons, Ltd.