Abstract: Methods for switching a mobile between operation in an mobile satellite system mode and a terrestrial wireless mode. When operating in the terrestrial wireless mode, the mobile terminal will initiate an attempt to switch into the MSS mode when it nears the boundary of the coverage area for a terrestrial wireless system to which it is registered. Conversely, a mobile terminal operating in the MSS mode will regularly attempt to switch into the terrestrial wireless mode. For both, a switch between modes is contingent on the mobile terminal identifying a suitable system for registration therewith upon completing the switch between modes. The criteria for identifying a suitable system for selection purposes include the following: (1) the selected system is available, i.e., the mobile terminal is physically located within a coverage area for the selected system; (2) the mobile terminal is compatible with the selected system; and (3) the selected system is willing to accept the mobile terminal.

Abstract: A massively parallel computer system is disclosed having a global router network in which pipeline registers are spatially distributed to increase the messaging speed of the global router network. The global router network includes an expansion tap for processor to I/O messaging so that I/O messaging bandwidth matches interprocessor messaging bandwidth. A route-opening message packet includes protocol bits which are treated homogeneously with steering bits. The route-opening packet further includes redundant address bits for imparting a multiple-crossbars personality to router chips within the global router network. A structure and method for spatially supporting the processors of the massively parallel system and the global router network are also disclosed.

Abstract: A massively parallel processor is provided with a plurality of clusters. Each cluster includes a plurality of processor elements ("PEs") and a cluster memory. Each PE of the cluster has associated with it an address register, a stage register, an error register, a PE enable flag, a memory flag, and a grant request flag. A cluster data bus and an error bus connects each of the stage registers and error registers of the cluster to the memory. The grant request flags of the cluster are interconnected by a polling network, which polls only one of the grant request flags at a time. In response to a signal on the polling network and the state of the associated memory flag, the grant request flag determines an I/O operation between the associated data register and the cluster memory over the cluster data bus. Both data and error bits are associated with respective processor elements. The sequential memory operations proceed in parallel with parallel processor operations.

Abstract: A parallel processor system which operates in a single-instruction multiple-data mode has a highly flexible local control capability for enabling the system to operate fast. The system contains an array of processing elements or PEs (12.sub.1 -12.sub.N) that process respective sets of data according to instructions supplied from a global control unit (20). Each instruction is furnished simultaneously to all the PEs. One local control feature (52) entails selectively inverting certain instruction signals according to a data-dependent signal. Another local control feature (48) involves controlling the amount of a bit shift in a barrel shifter (98) according to a data-dependent signal.

Abstract: The present invention provides a cephalosporin compound represented by formulas (I-S) and (I-R) ##STR1## wherein: R.sup.1 is a C.sub.1-4 alkyl, C.sub.3-4 alkenyl, C.sub.3-4 cycloalkyl, amino optionally substituted with a C.sub.1-4 alkyl radical, phenyl, or 2-,4- or 6- substituted phenyl group with two or fewer substitutents chosen from C.sub.1-4 alkyl, C.sub.1-3 alkoxy, halogen and hydroxy radicals;R.sup.2 is hydrogen or a C.sub.1-4 alkyl group;R.sup.a and R.sup.b, which should be different from each other, are hydrogen or a C.sub.1-4 alkyl group; andQ is N or CH,and the pharmaceutically acceptable non-toxic salts, physiologically hydrolyzable esters, hydrates and solvates thereof, which possess potent and broad antibacterial activities. The invention also provides processes for preparing these compounds and to pharmaceutical compositions containing them as active ingredients.

Abstract: The present invention relates to a cephalosporin compound including the pharmaceutically acceptable non-toxic salts, physiologically hydrolyzable esters, hydrates and solvates thereof of the formula(I) and its isomers: ##STR1## wherein: R.sup.1 is a C.sub.1-4 alkyl, C.sub.3-4 alkenyl, C.sub.3-4 alkynyl or --C(R.sup.3)(R.sup.4)COOH wherein R.sup.3 and R.sup.4, which may be the same or different, are hydrogen, C.sub.1-4 alkyl group, or constitute a C.sub.3-7 cycloalkyl group with the carbon atoms to which R.sup.3 and R.sup.4 are attached;R.sup.2, which may be attached to N.sup.a or N.sup.b, is a C.sub.1-4 alkyl, C.sub.3-4 alkenyl, C.sub.3-7 cycloalkyl, aryl or amino group; andQ.sub.1 and Q.sub.2, which may be the same or different, are CH or N.

Abstract: A massively parallel computer system is disclosed having a global router network in which pipeline registers are spatially distributed to increase the messaging speed of the global router network. The global router network includes an expansion tap for processor to I/O messaging so that I/O messaging bandwidth matches interprocessor messaging bandwidth. A route-opening message packet includes protocol bits which are treated homogeneously with steering bits. The route-opening packet further includes redundant address bits for imparting a multiple-crossbars personality to router chips within the global router network. A structure and method for spatially supporting the processors of the massively parallel system and the global router network are also disclosed.

Abstract: The lever assembly for a door lock comprises a door lock cylinder having a shank extended from each side of the door lock cylinder and two structure provided between the inside and outside lever and a door lock cylinder, respectively for resiliently returning and maintaining the levers in their horizontal positions. The returning and maintaining structure includes a spacer, a nut for fastening the spacer against the door lock cylinder, a mounting member for mounting a rotatable member, and a spring member cooperating with the rotatable structure and a retainer for holding the spring member, and a lever having a shaft fitted to the shank. The parts of the lever assembly are in turn fitted onto the shank in a cooperating relationship, thereby to resiliently return and maintain the lever in its original, horizontal position without tilting by using of the lever.

Abstract: A massively parallel processor includes an array of processor elements (20), of PEs, and a multi-stage router interconnection network (30), which is used both for I/O communications and for PE to PE communications. The I/O system (10) for the massively parallel processor is based on a globally shared addressable I/O RAM buffer memory (50) that has address and data buses (52) to the I/O devices (80, 82) and other address and data buses (42) which are coupled to a router I/O element array (40). The router I/O element array is in turn coupled to the router ports (e.g. S2.sub.-- 0.sub.-- X0) of the second stage (430) of the router interconnection network. The router I/O array provides the corner turn conversion between the massive array of router lines (32) and the relatively few buses (52) to the I/O devices.

Abstract: Two classes of systems for force-reflecting control that enable high force-reflection gain are presented: position-error-based force reflection and low-pass-filtered force reflection, both combined with shared compliance control. In the position-error-based class, the position error between the commanded and the actual position of a compliantly controlled robot is used to provide force reflection. In the low-pass-filtered force reflection class, the low-pass-filtered output of the compliance control is used to provide force reflection. The increase in force reflection gain can be more than 10-fold as compared to a conventional high-bandwidth pure force reflection system, when high compliance values are used for the compliance control.

Abstract: The present invention relates to new cephalosporin compounds of the formula(I), pharmaceutically acceptable non-toxic salts thereof, and physiologically hydrolyzable esters and solvates thereof, which have potent and broad antibacterial activities ##STR1## wherein R.sup.1 is a C.sub.1.about.4 alkyl, C.sub.3.about.4 alkenyl, C.sub.3.about.4 alkynyl group, or --C(R.sup.a)(R.sup.b)CO.sub.2 H.sub.1 wherein R.sup.a and R.sup.b are the same or different, and each is a hydrogen atom or a C.sub.1.about.4 alkyl group, or R.sup.a and R.sup.b form a C.sub.3.about.7 cycloalkyl group with the carbon atom to which they are linked;R.sup.2 is a C.sub.1.about.4 alkyl, C.sub.3.about.4 alkenyl or C.sub.3.about.4 cycloalkyl group, a substituted or unsubstituted amino group, or a substituted or unsubstituted phenyl group;R.sup.3 is hydrogen or a C.sub.1.about.4 alkyl group; andQ is N or CH.The invention further relates to a process for preparing said compounds, and to pharamaceutical compositions containing said compounds.

Abstract: In the present invention, 3,3-dimethyl-4-pentenoic acid (DPA) which is used for preparing permethric acid, an intemediate for preparing pyrethroid insecticides, is directly prepared from an isoprenol or a mixture of isoprenol and prenol without having to convert the isoprenol into a prenol or separate the mixture thereof into isoprenol and prenol. The present invention, therefore, has many advantages in view of yield, purity and procedure.

Abstract: The present invention provides certain novel cephalosporin derivatives represented by following formula(I), which are especially useful as intermediates for the preparation of cephalosporin compounds possessed with potent and broad antibacterial activities. ##STR1## wherein: R.sup.1 is a C.sub.1-4 alkyl, C.sub.3-4 alkenyl, C.sub.3-4 cycloalkyl, amino optionally substituted with a C.sub.1-4 alkyl radical, or phenyl group optionally substituted on its 2-, 4-and/or 6-position with a halogen, C.sub.1-4 alkyl, C.sub.1-3 alkoxy or hydroxy radical;R.sup.2 is hydrogen or a C.sub.1-4 alkyl group; andn is either 0 or 1.The invention also relates to processes for preparing these intermediates and their pharmacologically active cephalosporin antibiotics.

Abstract: A crystalline polyester resin derived from the reaction between a prepolymer and trimellitic anhydride in an amount of less than 10 wt % of the prepolymer where prepolymer as an intermediate product formed from the reaction between an alcohol mixture containing at least 40 mole % ethylene glycol and at least 30 mol % neopentyl glycol, and an acid mixture containing terephthalic acid or dimethyl terephthalate of at least 40 mole % and a linear dicarboxylic acid, or between an alcohol mixture containing 100 wt % terephthalic acid or dimethyl terephthalate. The crystalline polyester resin is very suitable for use in powder coating compositions and has a hyodroxyl number of 20 to 100, an average molecular weight of 1000 to 3500 and a melt viscosity at 160.degree. C. of 500 to 4000 cps as well as the characteristics of dense, regular, and repetitive structure.

Abstract: The present invention relates to novel cephalosporin compounds having high antimicrobial activity, which are shown by the formula(I), and to a process for preparing them ##STR1## wherein R.sup.1 is a hydrogen atom or an amino protecting group;R.sup.2 is acetoxy; andR.sup.3 is a hydrogen atom or a carboxyl protecting group (wherein when R.sup.2 contains quaternary ammonium, r.sup.2 and R.sup.3 may form a zwitter ion).The present invention also relates to the non-toxic and pharmaceutically acceptable salts of the cephalosporin compounds of the formula (I). Also described are compositions containing the antibiotics according to the present invention.