Organocatalytic Enantioselective Conjugate Addition of Malonic Acid Half Thioesters to Coumarin‐3‐carboxylic Acids Using N‐Heteroarenesulfonyl Cinchona Alkaloid Amides

We disclose herein an efficient enantioselective conjugate addition reaction between coumarin‐3‐carboxylic acids and malonic acid half thioesters (MAHTs). The reaction was catalyzed by N‐heteroarenesulfonyl Cinchona alkaloid amides to afford double‐decarboxylative conjugate addition products in good yield with high enantioselectivity. The reaction of various coumarin‐3‐carboxylic acids with MAHTs gave products in high yield with high enantioselectivity.

     

Direct Use of Benzylic Alcohols for Gold(III)‐Catalyzed S‐Benzylation of Mercaptobenzoic Acids in Water

We demonstrate the gold(III)‐catalyzed direct substitution of benzylic alcohols in water. These atom economic and environmentally benign protocols afford S‐benzylated products in moderate to excellent yields. In contrast, common Lewis or Brønsted acids as catalyst, and organic solvents such as dichloromethane or toluene were ineffective for the S‐benzylation of mercaptobenzoic acids. Water can be an attractive tool for new transition metal‐catalyzed reactions. A Hammett study for the rate constants with various substituted alcohols shows a good correlation (R²=0.97) between the log(k_X/k_H) and the σ⁺ value of the respective substituents. From the slope negative ρ values of 2.35 are obtained, suggesting that there is a build‐up of positive charge in the transition state. Our catalytic system can be performed with the use of only 2 mol% of gold(III) catalyst without any other additives in water, and scaled up to 10 mmol scale (85% isolated yield). Notably, the present method can accomplish the S‐benzylation of unprotected mercaptobenzoic acids, which is chemoselective and leaves the carboxyl group intact. Furthermore, the direct substitution of allylic and propargylic alcohols also proceeded smoothly in good yields.

     

Catalytic Aerobic Photo‐oxidation of a Methyl Group on a Heterocycle to Produce an Aldehyde via Homolytic C?I Bond Cleavage caused by Irradiation with Visible Light

A new catalytic method was developed for photo‐oxidizing the methyl group on aromatic heterocycles such as benzothiazole, benzoxazole, and quinoline to produce the corresponding aldehyde. This is the first report of the metal‐free catalytic synthesis of benzothiazole‐2‐carboxaldehydes using molecular oxygen as the terminal oxidant.

     

A field study on serum vitellogenin levels in male Reeves' pond turtles (Chinemys reevesii) from estrogen-contaminated sites and a reference site

To ascertain whether wild male turtles were influenced by environmental estrogens, we examined serum vitellogenin (VTG) levels of male Reeves' pond turtles (Chinemys reevesii) collected from four study sites (A-D) in Kyoto, Japan. Sites A-C, which were impacted by domestic or industrial wastewater and effluents from sewage treatment plants, were chosen as contaminated sites, and site D was intended as a reference site. This contaminated/reference site characterization was confirmed by measuring estrogenic activities of the water samples collected at each site for over a year. Serum VTG levels in the turtles were quantified by an enzyme-linked immunosorbent assay established previously. Estrogenic activities of the water samples were measured using a previously validated yeast two-hybrid assay and expressed as the estradiol-17beta equivalent. Estrogenic activity was observed at high levels at sites A-C, but was almost undetected at site D throughout the sampling period: the mean and range were 0.74 (<0.07-2.1), 0.52 (0.17-1.6), 1.7 (<0.07-7.3), and 0.07 (<0.07-0.62) ng/l at sites A-D, respectively. Significant differences were found only in site D versus sites A, B, and C. Therefore, site D and sites A-C were confirmed to be a reference site and contaminated ones, respectively. Overall, 320 male turtles were captured and examined. The majority of the turtles showed normal VTG values (0.10-0.74 microg/ml). Although only five turtles from sites A-C showed unusually high VTG values (1.1-5.9 microg/ml, nearly one order of magnitude higher than normal values but much lower than values in adult females), there was no significant difference in the incidence of these high values between sites A-C and site D. Moreover, among the five turtles, one turtle was captured again 2 months later, but its VTG value dropped to the normal level. The unusually high VTG values may therefore be transient elevation caused by incidental and/or individually specific agents. Excluding the unusually high values, the mean serum VTG (accompanied with the range) was 0.22 (0.10-0.74), 0.27 (0.11-0.62), 0.27 (0.17-0.68), and 0.23 (0.10-0.57) microg/ml at sites A-D, respectively. There were no significant differences in the mean VTG values among sites A-D. Although it should be clarified how and why the unusually high VTG values occurred at sites A-C, our results suggested that wild male C. reevesii turtles would not be significantly affected by xenobiotic estrogens at environmentally relevant levels in terms of serum VTG elevation.     

Investigation of reacting flow fields in miscible viscous fingering by a novel experimental method

The reacting flow fields in reactive miscible viscous fingering in a Hele‐Shaw cell studied by Nagatsu and Ueda had not been completely elucidated, mainly because one cannot exactly recognize where and when the reaction takes place in the reactive fingering pattern. We developed a novel experimental method that allowed us to identify the reaction region in the fingering pattern employed in the previous studies. The novel method involves switching of the less‐viscous liquid injected in both the nonreactive and reactive experiments. By using the novel method, we succeeded in showing how the reaction region in the fingering pattern was affected by the initial reactant concentrations, the Péclet number, and time. We propose physical models of the reacting flow field in the cell's gap direction that can explain the obtained experimental results. © 2009 American Institute of Chemical Engineers AIChE J, 2009     

Return Link Systems for Wireless Mobile Camera Using 42 GHz-Band with Frequency and Space Diversity Techniques

In this paper, return link systems for wireless mobile camera using 42 GHz-band in multipath fading environments are proposed. The return link systems for wireless mobile camera require wireless transmission with high reliability as same as the conventional wired camera systems. The proposed return link systems achieve transmission with high reliability by taking into consideration frequency and space diversity techniques. The proposed systems can be classified as 3 three types of return link systems according to diversity techniques： FD （frequency diversity） systems, SD （space diversity） systems and FD＋SD system （frequency and space diversity）. Computer simulations are carried out in order to confirm the effectiveness of the proposed return link systems. It is confirmed that the proposed three types of return link systems have an advantage about BER performances and effectively exploit frequency and space resources.     

Electrophoretic deposition of conjugated polymer: Deposition from dilute solution and PEDOT coating effect

It has been shown that the films of a soluble conjugated polymer poly[(9,9-dioctyl-2,7-divinylene fluorenylene)-alt-{2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene}] for electronic devices can be prepared by the electrophoretic deposition with polymer suspensions derived from dilute polymer solutions which are so dilute that the conventional spin-coating technique is not applicable. For example, a 100 nm-thick film can be prepared on an indium-tin-oxide (ITO) electrode from a suspension from solution containing 0.1 g/l of the polymer. The thickness of the polymer film deposited is found to be almost proportional to the concentration of the polymer, and the linearity down to 5.0 × 10^?3 g/l is confirmed. On the other hand, it has been found that coating the ITO electrode with poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) salt results in low and nonlinear deposition rate.     

Thermotropic and Barotropic Phase Behavior of Phosphatidylcholine Bilayers

Bilayers formed by phospholipids are frequently used as model biological membranes in various life science studies. A characteristic feature of phospholipid bilayers is to undergo a structural change called a phase transition in response to environmental changes of their surroundings. In this review, we focus our attention on phase transitions of some major phospholipids contained in biological membranes, phosphatidylcholines (PCs), depending on temperature and pressure. Bilayers of dipalmitoylphosphatidylcholine (DPPC), which is the most representative lipid in model membrane studies, will first be explained. Then, the bilayer phase behavior of various kinds of PCs with different molecular structures is revealed from the temperature–pressure phase diagrams, and the difference in phase stability among these PC bilayers is discussed in connection with the molecular structure of the PC molecules. Furthermore, the solvent effect on the phase behavior is also described briefly.