Abstract: The method is one of wireless transmission of information between two units consisting primarily of a portable object, such as a personalized watch (1), and a computer station (20). Each unit includes signal transmitting and/or receiving means (2, 24, 26) switched alternately to a transmitting mode and into a receiving mode. Information is transmitted by transmitting a plurality of information frames alternately between the two units. Each information frame comprises a synchronization field, which includes a particular number of synchronization bytes, an information packet and filler bytes. On receiving a frame, the receiving unit counts the synchronization bytes. The receiving unit transmits, in a heading of the information packet, a synchronization indication which is a function of the number of synchronization bytes received. The synchronization indication is used to correct the size of the synchronization field of the next frame received by the receiving unit.

Abstract: The method of synchronizing the analogue display (41) of a timepiece (40), including an electronic time base (64), is achieved using proximity sensors (60, 62) respectively associated with wheels (46, 48) each having an aperture (54, 56) for defining the angular position of the latter. Determination of the angular position of a wheel requires an angular distance of around 60° to 90° to be travelled with this type of proximity sensor. Dependency of the measurement results upon the temperature generates a problem of precision in determining the angular position of the wheels, in particular a wheel secured to the hour indicator, given that an angle of 60° to 90° corresponds to a time interval of 2 to 3 hours.

Abstract: The method of synchronising the analogue display (41) of a timepiece (40), including an electronic time base (64), is achieved using proximity sensors (60, 62) respectively associated with wheels (46, 48) each having an aperture (54, 56) for defining the angular position of the latter. Determination of the angular position of a wheel requires an angular distance of around 60° to 90° to be travelled with this type of proximity sensor. Dependency of the measurement results upon the temperature generates a problem of precision in determining the angular position of the wheels, in particular a wheel secured to the hour indicator, given that an angle of 60° to 90° corresponds to a time interval of 2 to 3 hours.

Abstract: The method is one of wireless transmission of information between two units consisting primarily of a portable object, such as a personalised watch (1), and a computer station (20). Each unit includes signal transmitting and/or receiving means (2, 24, 26) switched alternately to a transmitting mode and into a receiving mode. Information is transmitted by transmitting a plurality of information frames alternately between the two units. Each information frame comprises a synchronisation field, which includes a particular number of synchronisation bytes, an information packet and filler bytes. On receiving a frame, the receiving unit counts the synchronisation bytes. The receiving unit transmits, in a heading of the information packet, a synchronisation indication which is a function of the number of synchronisation bytes received. The synchronisation indication is used to correct the size of the synchronisation field of the next frame received by the receiving unit.

Abstract: A device of small dimensions includes a two coaxial wheels (4, 6) respectively including two plates (44, 46) parallel to each other. A sensor (10) including a detection element (14).formed by a magnetic or capacitive element, in particular a flat spiral coil, is provided for detecting the angular position of both of the two wheels. In order to do this, the sensor (10) detects the presence or absence of an active material above the detection element (14). For this purpose, each of plates (44) and (46) has at least one inactive region for the sensor and is formed at least partially of active material for the sensor. The sensor is arranged relative to the wheel the closest to the detection element in such a way that the latter is at least in part above or below said at least one inactive region in at least one determined angular position of said wheel so as to allow the sensor to detect the angular position of the wheel whose plate (44) is furthest from the detection element (14).

Abstract: A compound having the following general formula (I): ##STR1## where R is a hydrogen atom; a linear or branched C.sub.1 -C.sub.4 alkyl group, unsubstituted or substituted by at least a phenyl group or at least a hydrogen atom; a benzyl group substituted by at least a linear or branched C.sub.1 -C.sub.4 alkyl or alkoxy group or a nitro group; a silyl substituted by at least a linear or branched, unsubstituted or substituted C.sub.1 -C.sub.4 alkyl group; n is 0 or 1; and Y is a radical of formula ##STR2## wherein A is H, OH, Cl, CH.sub.2, CH.sub.2 X, where X is F, Cl, Br, I, OH or OR' and R' is COCH.sub.3 or a linear or branched, unsubstituted or substituted C.sub.1 -C.sub.4 alkyl group and - - - represents a single or a double bond, with the proviso that when n=0 and R is H, R' is not a methyl group.

Abstract: Cefazolin, cefazedone, cefoperazone, cefamandole, cefatrizine or ceftriaxone is prepared by reacting glutaryl 7-ACA of the formula: ##STR1## with a compound of formula (II):R--SH (II)wherein R is 5-methyl-1,3,4-thiadiazol-2-yl, 1H-1,2,3-triazol-4-yl, 1-methyl-tetrazol-5-yl or1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl group, and R.sup.1 and R.sup.2 are both hydrogen and the other is an acyl group, in an aqueous solution in an amount of 3-5 mols per mol of glutaryl 7-ACA to about 90.degree. C. and for a time from about 2 to about 10 hours;optionally recovering the excess of the compound of formula (II), thereby preparing a compound of formula (III) in an aqueous solution: ##STR2## wherein R is as above defined and optionally deacylating said compound of formula (III); andconverting the resulting compound of formula (I) ##STR3## wherein R, R.sup.1 and R.sup.2 are as defined above in the presence of a non-chlorinated solvent into one of said cephalosporins.

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 ##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.

Abstract: Timepiece including:a spring (1a) housed in said barrel (1),an electric power generator (2) coupled to said barrel (1),a rectifier circuit (4) connected to said generator, anda regulator circuit (6) supplied by the direct voltage (Ua) from the rectifier circuit and intended to control the rotational speed of the generator (2).

Abstract: There are disclosed new compounds of formula (I), wherein R is: a hydrogen atom: a linear or branched C1-C4 alkyl group, unsubstituted or substituted by at least a phenyl group or at least a hydrogen atom: a benzyl group substituted by at least a linear or branched C1-C4 alkyl or alkoxy group or a nitro group; a silyl substituted by at least a linear or branched, unsubstituted or substituted C1-C4 alkyl group; n is 0 or 1; and Y is a radical of formula (II), wherein A is H, OH, Cl, CH2, CH2X, where X is F, Cl, Br, I, OH or OR' and R' is COCH3 or a linear or branched, unsubstituted or substituted C1-C4 alkyl group and . . . represents a single or a double bond, with the proviso that when n=0 and R is H, R' is not a methyl group; and processes for obtaining them.

Abstract: The timepiece comprises an electrical energy generator (3) comprising a rotor (3a) and means (3b) for supplying said electrical energy in response to rotation of said rotor (3a), a source of mechanical energy (2), measuring means (Trig) coupled to said generator (3) for producing measurement pulses of the angular frequency of an alternating voltage supplied by the generator (3), braking means (K) responsive to a braking command signal for applying a braking torque to said rotor (3a), an electronic circuit (1) comprising reference means (Osc) for producing a reference signal (FR), and slaving control means (Div, Cmp, Tmr) arranged to control said braking means (K) when said measurement pulses are ahead with respect to the reference signal.

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.

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.