Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt.

Egis Gyogyszergyar

Robert Boschgmbh

Telefonaktiebolaget Lm Ericsson (publ)

Egis Gyogyszergyar Rt.

Taurus Gumiipari Vallalat

Muanyagipari Kutato Intezet

Zoltek Companies, Inc.

Gabor Kovacs

Istvan Stadler

Istvan Szekely

Sandor Virag

Agnes Horvath

Peter S Kormoczy

Istvan Hermecz

Vilmos Simonidesz

Istvan Tomoskozi

Judit Sipos

Tamas Szuts

Maria Balogh

Peter Ritli

Aniko Pajor

Marianna Lovasz Nee Gaspar

Csaba Szantay

Dezso Korbonits

Geza Kereszturi

Jozsef Ivanics

Geza Galambos

Antal Simay

Lelle V Vasvari Nee Debreczy

Rudolf Soos

Pal Hadhazy

Bela Koszegi

Pal Kiss

Gyula Sebestyen

Gergely Heja

Katalin Marmarosi Nee Kellner

Sandor Botar

Jeno Marton

Karoly Horvath

Gyorgy Dorman

Peter Gyory

Lajos T Nagy

Imre Moravcsik

Tibor Szabo

Laszlo Tardos

Kalman Takacs

Endre Palosi

Peter Szentmiklosi

Gabor Horvath

Kalman Nagy

Gyula Papp

Zoltan Zubovics

Lelle Vasvari

Vera Gergely

Laszlo Szekeres

Csaba Gonczi

Sandor Antus

Lajos Novak

Laszlo Institoris

Gyorgy Krasznai

Agnes Gottsegen

Karoly Kanai

Ferenc Szederkenyi

Emil Minker

Lajos Toldi

Ilona K Ajzert

Gyula Simig

Lajos Szabo

Jozsef Knoll

Jozsef Szejtli

Zoltan Meszaros

Gabor Gigler

Gabor T Szabo

Gabor Blasko

Bela Bertok

Katalin Marmarosi

Pal Fekete

Laszlo Pallos

Istvan Tibor Toth

Daniel Bozsing

Ida Szvoboda Nee Kanzel

Imre Bata

Tamas U Kallay

Antal Gajary

Katalin Szemeredi

Maria Szomor Nee Wundele

Andras Egyed

Laszlo Ledniczky

Tamas Szabolcsi

Jozsef Gaal

Mihaly Nogradi

Judit Cser Nee Kun

Klara Gyires

Gyorgy Somogyi

Laszlo Palotas

Jozsef Lengyel

Peter L Nagy

Judit Kun

Laszlo Fesus

Istvan Pallagi

Gyula Dalmadi

Margit Csorgo

Peter Literati Nagy

Matyas Szentivanyi

Jozsef Nemes

Lorand Debreczeni

Ildiko Szilagyi

A method for training a style encoder of a neural network. Sensory input variables, which represent a movement of a system and surroundings of the system, are compressed to an abstract driving situation representation in at least one portion of a latent space of the neural network, using a trained situation encoder of the neural network. The sensory input variables are compressed to a driving style representation in at least one portion of the latent space, using the untrained style encoder. The driving style representation and the driving situation representation are decompressed from the latent space to output variables, using a style decoder of the neural network. A structure of the style encoder is changed to train the style encoder until the output variables of the style decoder represent the movement.

Method and device for training a style encoder of a neural network and method for generating a driving style representation representing a driving style of a driver

A spliced fiber tow () having a uniform density along its entire length is provided. The spliced fiber tow is manufactured by rarefying the ends () of the two fiber tow segments to be joined, aligning the rarefied regions () and then applying pressurized gas to entangle the filaments in the rarefied regions. An apparatus () for forming the spliced fiber tow includes a pair of rarefying blades () and an entanglement element ().

Spliced carbon fiber tow and splicing method

The present invention relates to a receiver in a 2&#xd7;2 Line of Sight Multiple Input Multiple Output, LoS MIMO, system. The receiver is arranged to estimate a first (&#x15c;) and a second (&#x15c;) signal on the basis of a first (r(t)) and a second (r(t)) signal received from respective first and second transmitters (Tx,Tx). Said received signals (r(t), r(t) comprises a first and second signal. The receiver comprises a first Phase Locked Loop (), PLL, and a second PLL (), which are arranged to respectively determine a first (In) and second (In) demodulated signal from the first (r(t)) and the second (r(t)) received signals. The receiver further comprises an equalizer () which is arranged to estimate the first (&#x15c;) and second (&#x15c;) signals from the demodulated signals (In,In). The receiver is particularly characterized in that the equalizer () further is arranged to compensate for an independent rotation frequency ftrftr, where ftrand ftrare the respective deviations from the nominal frequency values of a first and a second transmitted signals comprising the first and second signals.

Apparatus for performing channel equalization on a MIMO signal

This invention relates to new oxaindene derivatives, a process for the preparation thereof and pharmaceutical compositions comprising the same. The compounds according to the invention are characterized by the general formula (1) ##STR1## wherein R.sup.1 represents lower C.sub.1-4 alkyl, lower C.sub.1-4 alkoxy or lower C.sub.3-6 cycloalkyl,

Oxaindene derivatives and process for the preparation thereof

The invention relates to a new process for the preparation of compounds of the Formula I ##STR1## (wherein R stands for hydrogen or methyl) and pharmaceutically acceptable salts thereof which comprises reacting a compound of the Formula V ##STR2## (wherein R.sup.1 and R.sup.2 stand for an aliphatic acyloxy group comprising 2-6 carbon atoms and optionally substituted by halogen: or for an aromatic acyloxy group comprising 7-11 carbon atoms) with an amine of the Formula VI ##STR3## (wherein R has the same meaning as stated above) or a salt thereof and subjecting the compound of the Formula VII ##STR4## thus obtained (wherein R, R.sup.1 and R.sup.2 are as stated above) to hydrolysis after or without isolation and if desired converting the compound of the Formula I thus obtained into a salt thereof or setting free the same from its salt. The compounds of the Formula I are known antibacterial agents.

Process for the preparation of quinoline carboxylic acids

A method of using a compound of the Formula (V) ##STR1## or a pharmaceutically acceptable salt thereof is disclosed, wherein R.sup.1 and R.sup.2 are each C.sub.1 to C.sub.6 aliphatic acyloxy, unsubstituted or substituted by halogen, or are each C.sub.7 to C.sub.11 aromatic acyloxy, for preventing amination of the 6-position when a compound of the Formula (I) ##STR2## or a pharmaceutically acceptable salt thereof is to be formed, which comprises the steps of:

Process for the preparation of quinoline carboxyolic acids

The invention relates to an improved process for the preparation of 2,2-dimethyl-5-(2,5-dimethylphenoxy)-pentanoic acid of Formula (I) ##STR1## which comprises reacting an ester of the general Formula (X) ##STR2## wherein X represents halogen and Z stands for a straight or branched chain C.sub.1-8 alkylene group optionally substituted by one or two 2,2-dimethyl-5-halopentanoyloxy group(s), wherein halo represents chlorine or bromine, and in which alkylene group one or two methylene group(s) may be optionally replaced either by hetero atom(s) or by a bivalent heterocyclic group--with an alkali salt of 2,5-dimethylphenol of Formula (II) ##STR3## or with an ester of the latter formed with a lower alkanoic acid, and hydrolizing the aryloxy-substituted ester of the general Formula (XI) thus obtained. ##STR4## Furthermore the invention relates to intermediate compounds of the general Formula (X), wherein X and Z are as stated above, and to a process for the preparation thereof.

Process for the preparation of

The invention relates to an improved process for the preparation of 2,2-dimethyl-5-(2,5-dimethylphenoxy)-pentanoic acid of Formula (I) ##STR1## which comprises reacting an ester of the general Formula (X) ##STR2## wherein X represents halogen and Z stands for a straight or branched chain C.sub.1-8 alkylene group optionally substituted by one or two 2,2-dimethyl-5-halopentanoyloxy group(s), wherein halo represents chlorine or bromine, and in which alkylene group one or two methylene group(s) may be optionally replaced either by hetero atom(s) or by a bivalent heterocyclic group--with an alkali salt of 2,5-dimethylphenol of Formula (II) ##STR3## or with an ester of the latter formed with a lower alkanoic acid, and hydrolizing the aryloxy-substituted ester of the general Formula (XI) thus obtained. Furthermore the invention relates to intermediate compounds of the general Formula (X), wherein X and Z are as stated above, and to a process for the preparation thereof.

The invention relates to novel diphenylpropylamine derivatives of the general formula (I). ##STR1## R.sup.1 stands for hydrogen or a methyl group; R.sup.2 stands for hydrogen, a methyl or n-decyl group;

Diphenkylpropylamines for the therapy of heart disease

The invention relates to a new process for the preparation of compounds of the Formula I ##STR1## (wherein R stands for hydrogen or methyl) and pharmaceutically acceptable salts thereof which comprises reacting a compound of the Formula V ##STR2## (wherein R.sup.1 and R.sup.2 stand for an aliphatic acyloxy group comprising 2-6 carbon atoms and optionally substituted by halogen; or for an aromatic acyloxy group comprising 7-11 carbon atoms) with an amine of the Formula VI ##STR3## (wherein R has the same meaning as stated above) or a salt thereof and subjecting the compound of the Formula VII ##STR4## thus obtained (wherein R, R.sup.1 and R.sup.2 are as stated above) to hydrolysis after or without isolation and if desired converting the compound of the Formula I thus obtained into a salt thereof or setting free the same from its salt. The compounds of the Formula I are known antibacterial agents. The advantage of the process of the present invention is that it makes the desired compounds of the Formula I available in a simple manner, with high yields and in a short reaction time.

1-Methylamino-quinoline-carboxylic acid derivatives

The invention relates to novel racemic or optically active berban derivatives of the formula (I) ##STR1## wherein R.sup.1 and R.sup.2 represent independently from the other a hydroxyl, straight or branched chain alkoxy group 1 to 6 carbon atoms or R.sup.1 and R.sup.2 together represent a C.sub.1-3 alkylenedioxy group;

Berban derivatives as .alpha..sub.2 -adrenergic antagonists

The invention relates to new oxidiazole-alkyl-purine-derivatives of the Formula I ##STR1## and pharmaceutically acceptable salts thereof wherein A stands for C.sub.1-4 alkylene and

Oxadiazole-alkyl-purine derivatives useful as antitussive agents

The invention relates to a transdermal laminated pharmaceutical composition (plaster) having prolonged effect, wherein one or more storing layer(s) comprising the active ingredient, an ethylene/vinyl acetate copolymer regulating layer and an adhesive layer are applied onto the carrier. The pharmaceutical composition is prepared by coupling a carrier comprising the active ingredient with a regulating layer consisting of an ethylene/vinyl acetate copolymer foil having a vinal acetate content of 2-40 molar %. The foil is previously irradiated in a thickness of 100-300 .mu.m with a high-energy irradiation in a dose of 1-15 Mrad--preferably with electrone radiation--and thereafter stretched at 80.degree.-90.degree. C. to a thickness of 2-200 .mu.m. The system comprising the carrier and the regulating layer is subsequently coupled with an adhesive layer.

Transdermal laminated pharamaceutical compositions having prolonged

Boric anhydrides of

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Budapest, Hungary

Gabor Kovacs