Abstract: A fluid-type multiple electrochemical system. The system includes a substrate for an electric circuit having a plurality of electrode parts formed at regular intervals. The electrode parts each include a reference electrode and an auxiliary electrode. Also provided is a fluid-type substrate having a fluid injection part, a fluid ejection part and a plurality of fluid storages. The fluid storages are formed at the same regular intervals as the electrode parts of the substrate and are connected with each other through fluid passages. The system also includes a sensor substrate having a plurality of unit sensors formed at the same regular intervals as the electrode parts of the substrate. Each unit sensor has an electrode part, an electrode pad for supplying power voltage simultaneously, and an electrode wiring.

Abstract: Organoiodonium salts, including certain novel symmetrical and unsymmetrical diaryliodonium;. polyiodonium and cyclic iodonium salts are synthesized by a significantly improved electrochemical coupling reaction which provides greater control and selectivity over the end product produced. Reaction mixtures comprising aryliodides and/or aromatic substrates are electrolyzed in novel reaction mediums comprising strong acid electrolyte, lower carboxylic acid, and preferably in the presence of acid anhydride in amounts >10 percent by-weight, and up to 50 percent by-weight or more, to provide a high degree of product selectivity, and at yields which can even be quantitative. The methods are conducted by introducing the electrolysis reaction mixture into an undivided electrochemical cell equipped with a cathode and preferably a conductive carbon anode.

Abstract: A process for the preparation of chiral 2-aryl or 2-heterocyclyl-propionic acids of the formula wherein the substituents are as defined in the specification.

Abstract: The present invention provides a process for preparing an exo-methylenepenam compound represented by the general formula (5) characterized in that a &bgr;-lactam halide compound represented by the general formula (2) is subjected to an electroreduction process to obtain the exo-methylenepenam compound.

Abstract: A main body of a NOx sensor has a sensor cell and defines a reference gas chamber and a sample gas chamber therein. The sample gas chamber has a wall formed by a solid electrolytic substrate having an oxygen ion conductivity. The sensor cell is disposed between the reference gas chamber and the sample gas chamber for detecting a concentration of a NOx gas. A pump cell body of the NOx sensor has a surface facing to the sample gas chamber and has a pump cell for introducing and exhausting an oxygen gas to and from the sample gas chamber. In manufacturing this NOx sensor, the main body and the pump cell body are fabricated individually as separate items. The main body and the pump cell body are sintered independently. Then, the main body and the pump cell body are assembled into to the NOx sensor.

Abstract: A process for preparing a 3-alkoxymethylcephem compound represented by the formula (II) ##STR1## where R.sub.1 is a hydrogen atom, amino or protected amino, R.sub.3 is a hydrogen atom or carboxylic acid protective group and R.sub.4 is lower alkyl, which process is characterized in that a 3-thiomethylcephem compound represented by the formula (I) ##STR2## where R.sub.1 and R.sub.3 are as defined above and R.sub.2 is aryl which may have a substituent, is electrolytically oxidized in an electrooxidation reaction system in the presence of a lower alcohol using as a positive electrode, a material selected from the group consisting of platinum, tin, aluminum, stainless steel, nickel, lead oxide, carbon, iron oxide and titanium, to obtain the 3-alkoxymethylcephem compound.

Abstract: A process for synthesizing the compounds ##STR1## wherein X is halo, consists of, at a minimum, electrochemical oxidation of the allyl acetonide reactant with halide salt in an aqueous system, the desired compounds being useful as intermediates for the synthesis of inhibitors of renin or HIV protease or other proteases.

Abstract: A process is described for preparing 3-exomethylene cephalosporanic acid derivatives for use in the synthesis of cephalosporin antibiotics such as ceftibuten. The process comprises electrochemical reduction of a compound of the formula (IV) ##STR1## wherein: R.sup.3 is CH.sub.3 C(O)--; ##STR2## is an optional sulfoxide group; n is 2 or 3; R.sup.1 is H and R is H or NHR.sup.2, where R.sup.2 is H or a protecting group selected from C.sub.6 H.sub.5 CH.sub.2 OC(O)--, C.sub.6 H.sub.5 C(O)-- or C.sub.1 -C.sub.6 alkoxy-C(O)--; or wherein R and R.sup.1 together with the carbon atom to which they are attached comprise --C(O)--, and produces the desired 3-exomethylene compounds with low levels of the corresponding 3-methyl tautomers.