Studies on 1-Deoxynojirimycin-Containing Glycans: Synthesis of Novel Disaccharides Related to Lactose,Lactosamine, and Chitobiose

Abstract

Suitably protected 1-deoxynojirimycin (l, 5-dideoxy-l, 5-imino-D-glucitol; DNJ) and its 2-acetamido derivative, i.e., 2, 3, 6-tri-O-benzyl-.N-benzyloxycarbonyl-l, 5-dideoxy-1, 5-imino-D-glucitol (6) and 2-acetamido-3, 6-di-O-benzyl-N-benzyloxycarbonyl-1, 2, 5-trideoxy-l, 5-imino-D-glucitol (14) were each coupled with methyl 2, 3, 4, 6-tetra-O-acetyl-1-thio-β-D-galactopyranoside (15) in the presence of dimethyl(methylthio)-sulfonium triflate (DMTST) as a promoter, to give 16 and 18, which were converted to the novel disaccharides (20, 21) related to lactose and lactosamine. Coupling of 14with methyl 3, 4, 6-tri-O-acetyl-2-deoxy-2-phthalimido-l-thio-β-D-glucopyranoside (22) gave achitobiose analog (25). O-(β-D-Galactopyranosyl)-(l→3)-DNJ derivatives (38, 39) and O-(β-D-glucopyranosyl)-(l→3)-DNJ (45) were also synthesized. Conformational analysis of a variety of DNJ derivatives, based on the ¹H NMR data, is also discussed.     

Laser-diode pumped heavy-doped Yb:YAG ceramic lasers

Laser performance of heavy-doped Yb:YAG ceramics was investigated using a two-pass pumping miniature laser configuration. Slope efficiency of 52% and optical-to-optical efficiency of 48% have been achieved for 1-mm-thick YAG ceramic doped with 20 at.% ytterbium ions. Laser spectra of Yb:YAG ceramic and single-crystal lasers were addressed under different intracavity laser intensities. Heavy-doped Yb:YAG ceramic is more suitable for a thin disk laser than a single-crystal with the same Yb(3+)-ion lasants.     

Catalytic Activity of Molecular Rhenium Sulfide Clusters [Re6S8(OH)6−n (H2O) n ](4−n)− (n = 0, 2, 4, 6) with Retention of the Octahedral Metal Frameworks: Dehydrogenation and Dehydration of 1,4-Butanediol

A series of molecular rhenium sulfide clusters [Re₆S₈(OH)_6?n (H₂O) _n ]^(4?n)? (n = 0, 2, 4, 6) catalyze dehydrogenation of alcohols, and hydrogenation of ketones and olefins in a hydrogen stream at 350 °C. The catalytic activities of the dianionic and neutral clusters (n = 2, 4) are lower than those of tetraanionic and dicationic clusters (n = 0, 6) for all the reactions. When 1,4-butanediol is allowed to react over K₄[Re₆S₈(OH)₆], dehydrogenation proceeds to yield 2-hydroxytetrahydrofuran and successively γ-butyrolactone above 300 °C. Over [Re₆S₈(H₂O)₆]SO₄ dehydration proceeds to yield tetrahydrofuran above 250 °C. The thermal activation mechanisms of these clusters were studied by powder X-ray diffraction analyses, Raman spectrometry, extended X-ray absorption fine structure spectrometry, thermogravimetry, and differential thermal analyses. The catalytically active site of K₄[Re₆S₈(OH)₆] is an uncoordinated metal site (Lewis acid site) developed by the loss of a water molecule from two hydroxo ligands. The active site of [Re₆S₈(H₂O)₆]SO₄ is a Brønsted acid site; the anhydrous aqua cluster dication disproportionates to a hydroxo cluster monocation and a proton. Both of the octahedral cluster frameworks are retained up to 500 °C.     

Direct Asymmetric Mannich‐Type Reaction of α‐Isocyanoacetates with Ketimines using Cinchona Alkaloid/Copper(II) Catalysts

The enantioselective direct Mannich‐type reaction of ketimines with α‐isocyanoacetates has been developed. Excellent yields and enantioselectivity were observed for the reaction of various ketimines and α‐isocyanoacetates using cinchona alkaloid/Cu(OTf)₂ and a base. Both enantiomers of the products could be obtained by using pseudoenantiomeric chiral catalysts. This process offers an efficient route for the synthesis of α,β‐diamino acids.     

pH-responsive non-surface-active/surface-active transition of weakly ionic amphiphilic diblock copolymers

The weakly ionic amphiphilic diblock copolymer polystyrene-b-poly(acrylic acid) was synthesized by nitroxy radical-mediated living radical polymerization with precise control of block length, block ratio, and polydispersity. Systematical surface tension experiments and foam formation observations revealed that this polymer was non-surface active under neutral and alkaline (pH 10) conditions, while it was surface active under an acidic condition (pH 3). This result supports our proposed origin of non-surface activity; the image charge repulsion at the air/water interface is essential in addition to very stable micelle formation in the bulk solution. At a higher pH (pH 12), the polymer showed slight surface activity since the added NaOH played a role as an added salt. The critical micelle concentration (cmc) was estimated by static light scattering. Cmc increased with increasing added salt (NaCl) concentration as was observed for other strongly ionic non-surface-active polymers. Hence, this trend is characteristic for non-surface-active polymers. The pH dependence of cmc was minimum at pH 8–10. Since the acrylic acid block is fully ionized under this condition, the strong image charge repulsion at this condition accelerated micelle formation at a low polymer concentration, which consequently decreased cmc. Micelles in bulk solution were confirmed by dynamic light scattering, and the salt concentration and pH dependencies of the hydrodynamic radius of the micelles were also estimated. The pH-responsive non-surface-active/surface-active transition observed in this study strongly supports the fact that the image charge repulsion is an essential factor for non-surface activity in addition to stable micelle formation in solution.     

Electrochemical Sensing of Ovalbumin Based on the Interaction between Lysozyme Origin/Tyrosine‐rich Peptides Modified on Magnetic Beads and Oligothreonine/Ovalbumin‐origin Peptide

We developed a highly sensitive electrochemical system for the sensing of ovalbumin (OVA). Lysozyme origin/tyrosine‐rich peptides (RNRCKGTDVQAWY₄C) were immobilized on magnetic beads, and the competitive reaction between OVA and oligothreonine/OVA origin peptide probe (T₈VLLPDEVSG) could then be measured. In a previous study, the detection of OVA at the 10^?13 M level was achieved using RNRCKGTDVQAWY₄C‐modified beads via a cross‐linker. To improve the sensitivity to OVA, this system uses T₈VLLPDEVSG peptide probe to measure the interaction to RNRCKGTDVQAWY₄C immobilized on magnetic beads. The peak of Y₄C actually was an electron‐transfer peptide, which represented the oxidation of a phenolic hydroxyl group. First, we confirmed that the oxidation response of Y₄C was increased based on an improvement in the electron transfer accessibility by oligothreonine. Next, T₈VLLPDEVSG peptide probe was used for the electrochemical sensing of OVA in solutions that contained consistent amounts of RNRCKGTDVQAWY₄C on magnetic beads. As a result, the peak current decreased as the concentration of OVA increased. The sensitivity to OVA was improved compared with the use of only RNRCKGTDVQAWY₄C on magnetic beads. The OVA detection level was 10^?14 M, which approximates the results from antibody‐antigen reactions. Consequently, the proposed system is a powerful new concept in protein sensing.     

Catalytic Carbonylation and Carboxylation of Organosulfur Compounds via C−S Cleavage

Transition‐metal‐catalyzed carbonylation with CO gas occupies a privileged position in organic synthesis for the synthesis of carbonyl compounds. Although this attractive and useful chemistry has led many researchers to investigate carbonylative transformations of various organic (pseudo)halides, C?S‐cleaving carbonylation of organosulfur compounds has been fairly limited. Recently, a broad spectrum of C?S‐cleaving transformations has been emerging in the field of cross‐coupling. In light of the importance of carbonyl compounds as well as considerable advancement for employing organosulfur compounds as competent surrogates of (pseudo)halides, carbonylative transformations of C?S bonds should be of high value. This Minireview focuses on catalytic C?S carbonylation of organosulfur compounds with CO or its equivalents. In addition, reductive carboxylation of C?S bonds with CO₂ is described.     

Palladium‐Catalyzed C−H Iodination of Arenes by Means of Sulfinyl Directing Groups

C?H iodination of aromatic compounds has been accomplished with the aid of sulfinyl directing groups under palladium catalysis. The reaction proceeds selectively at the peri‐position of polycyclic aryl sulfoxides or at the ortho‐position of phenyl sulfoxides. The iodination products can be further converted via iterative catalytic cross‐coupling at the expense of the C?I and C?S bonds. Computational studies suggest that peri‐C?H palladation would proceed via a non‐directed pathway, wherein neither of the sulfur nor oxygen atom of the sulfinyl group coordinates to the palladium before and at the transition state.     

Full fitting analysis of the relative intermediate form factor measured by neutron spin echo

This paper describes the dynamics of a water-in-oil microemulsion from the dilute to the dense droplet region. Using the relative intermediate form factor method for neutron spin echo data analyses [M. Nagao, H. Seto, Phys. Rev. E 78 (2008) 011507], the shape and structure fluctuations of a droplet microemulsion are successfully decoupled. In the previous paper, we used the first cumulant analysis of the shape fluctuation model, while the full fitting form of the same model is applied in this paper. The final results of the fittings using the first cumulant approximation and the full form of the model are almost identical, and therefore, the validity of the method is strengthened. The estimated bending modulus of the surfactant membrane, κ, is basically the same, within the experimental errors, in the previous and present results. The κ is not affected much by an increase of the droplet concentration. A clear dynamic slowing down of the water droplets is highlighted at the length scale corresponding to the inter-droplet distance from the structure fluctuation analysis.