Nippon Kayaku Kabushiki Kaisha

Microsoft Technology Licensing, LLC

Elpida Memory, Inc.

Toray Industries, Inc.

Teijin Limited

Nikon Corporation

Shigeru Aoki

Toru Takagi

Tadashi Shirai

Koji Miyata

Hiroshi Ohki

Kiyonori Oyu

Kazuya Okamoto

Isao Sugaya

Wataru Funamizu

Rinzo Nishizawa

Takashi Nagashima

Akikazu Mitsunobu

Kenichiro Tanaka

Hajimu Kurumatani

Osamu Saruwatari

Makoto Tsuda

Sota Nakanishi

Yasuhisa Tashiro

Yojiro Tezuka

Masashi Okada

Ryoichi Hasegawa

Naoki Ohkouchi

Yoshinobu Miyazawa

Tasuku Okamoto

Tadashi Fujii

Mamoru Katagiri

Toshiro Narita

Azmee Carlton Lane

Noriko Ooishi

Michimune Kono

Hiroshi Yagiuchi

Atsushi Osaki

Shintaro Nishida

Masaharu Shiga

Yuka Saito

Yuji Kuwabara

Kunio Iwasaki

Yuzo Aboshi

This vehicle of monocoque construction is formed by fastening together resin parts which are an upper body integrally made of a transparent thermoplastic resin composition, a lower body integrally made of a thermoplastic resin composition and a floor integrally made of a thermoplastic resin composition, wherein the vehicle is characterized in that the lower body is provided with a flange part rising up from the entire perimeter of the bottom surface and, in the center of the bottom surface, a convex rib part that continues rearward from the front of the vehicle, and the upper body and the floor being fastened to the flange part and the convex rib part of the lower body. In so doing, there can be provided a vehicle which is lightweight, affords a good field of view during driving, is simple in construction, and has the necessary rigidity.

Vehicle of monocoque construction formed from thermoplastic resin members

Techniques are disclosed herein for processing iTV. A request to play a first interactive television signal at a first electronic device is received. A first virtual machine for processing the first interactive television signal is instantiated at the first electronic device. A first file that includes information associated with playing interactive TV on the first electronic device is accessed from non-volatile storage on the first electronic device. A request to play a second interactive television signal at a second electronic device that is communicatively coupled to the first electronic device is received. A second virtual machine for processing the second interactive television signal is instantiated at the first device. A second file that includes information associated with playing interactive TV on the second electronic device is stored in non-volatile storage on the first electronic device.

Concurrent interactive television for network connected devices

A hybrid tuner, comprising multiple individual tuners having differing capabilities of receiving programs or channels of broadcast audio or video content, can be controlled by periodically determining the capabilities of each individual tuner to receive broadcast channels, storing such information into a guide database and then utilizing such information to select appropriate individual tuners to tune in desired programs. If the tuners that can receive a desired program are already in use, the program they are currently receiving can be switched to a different tuner to free up the tuner that can receive the desired program without interrupting the consumption of the program currently being received. When determining the capabilities of an individual tuner to receive a particular channel, one or more tokens associated with such a channel, and utilized to prevent unauthorized access to such a channel, can be obtained from the guide database and provided to the tuner.

Hybrid tuner control

The present invention has an object to provide a semiconductor chip of high reliability with less risk of breakage. Specifically, the present invention provides a semiconductor chip having a semiconductor silicon substrate including a semiconductor device layer and a porous silicon domain layer, the semiconductor device layer being provided in a main surface region on one surface of the semiconductor silicon substrate, the porous silicon domain layer being provided in a main surface region on a back surface which is the other surface of the semiconductor silicon substrate, and the porous silicon domain layer having porous silicon domains dispersed like islands in the back surface of the semiconductor silicon substrate.

Semiconductor chip having island dispersion structure and method for manufacturing the same

A method of treatment for diabetic neuropathy using combined administration of a formulation including as an active ingredient a prostaglandin I derivative, especially a prostaglandin I.sub.2 derivative with an anti-diabetic agent is applied to hypofunction of motor nerve and sensory nerve to which conventional anti-diabetic agents do not provide sufficient treatments, with nerve conduction velocities improved.

Method of treatment for diabetic neuropathy

The present invention relates to a process for producing .alpha.-aspartyl-phenylalanine ester represented by the general formula ##STR1## wherein R' represents an alkyl group having 1 to 4 carbon atoms, by reducing an N-protected-N-hydroxymethyl-.alpha.-aspartyl-phenylalanine ester represented by the general formula ##STR2## wherein R represents an organic mioety which can be substituted reductively by hydrogen, and R' is as defined above, with hydrogen gas or formic acid, in the presence of a reduction catalyst and an aromatic primary amine. According to the present invention, there can be obtained a high purity .alpha.-aspartyl-phenylalanine ester with a high yield.

Process for producing .alpha.-aspartyl-phenylalanine ester

This invention relates to a process for producing optically active valine, characterized by optically resolving DL-valine hydrochloride in a solvent containing an amine salt, a sulfonic acid or a carboxylic acid and isolating optically active valine after the decomposition of the obtained optically active valine hydrochloride.

Process for producing optically active valine

This invention relates to a process for producing optically active phenylalanine, characterized by optically resolving DL-phenylalanine.optically active mandelic acid complexes in an aqueous solvent in the presence of an acidic compound having a pKa value of 0.90 to 2.10 and isolating optically active phenylalanine from the obtained optically active phenylalanine.optically active mandelic acid complex. According to the process of the present invention, it is possible to decrease the amount of a mother liquor of resolution to 1/5 to 1/10 of that when no acidic compound is used and to obtain optically active phenylalanine having an optical purity of as high as 96.5% or above without a step of optical purification when optically active phenylalanine is isolated from the obtained optically active phenylalanine.optically active mandelic acid complex.

Process for producing optically active phenylalanine

The present invention relates to a process for preparing optically active phenylalanine which comprises resolving mixture of a complex of D-phenylalanine and optically active mandelic acid and a complex of L-phenylalanine and optically active mandelic acid in a solvent containing hydrochloric acid, carboxylic acid, phosphoric acid or a salt thereof to obtain the complex having lower solubility, and removing said optically active mandelic acid from the obtained complex to obtain an optically active phenylalanine. In the case of resolving DL-phenylalanine by the process according to the present invention, the amount of mother liquor used in resolution can be made to about 1/2 to 1/6 as compared to the amount of mother liquor of which the acidic compound or the salt thereof is not used in the resolution. Accordingly, the process according to the present invention is extremely profitable as an industrial process for producing an optically active phenylalanine.

Process for preparing optically active phenylalanine

Two optically active amino acid-mandelic acid complexes are obtained by interacting in a solvent under pH conditions of 1.0-4.0 an amino acid expressed by a general formula ##STR1## (in which R represents a methyl group, an ethyl group or a methylthioethyl group) and mandelic acid, one of the acids being an optically active substance and the other being a racemic modification, and optically resolving the resulting complexes into two diastereoisomers by using solubility difference therebetween. The optically active complexes are each decomposed by means of an acid, a strongly acidic ion-exchange resin, or a weakly basis ion-exchange resin to obtain optically active amino acids or optically active mandelic acid.

Process for preparing optically active amino acid or mandelic acid

Two optically active amino acid-mandelic acid complexes are obtained by reacting in a solvent under pH conditions of 1.0-4.0, an amino acid expressed by a general formula ##STR1## (in which R represents a methyl group, an ethyl group or a methylthioethyl group) and mandelic acid, one of the acids being an optically active substance and the other being a racemic modification, and optically resolving the resulting complexes into two diastereomers by using a solubility difference therebetween. The optically active complexes are each decomposed by means of an acid, a strongly acidic ion-exchange resin, or a weakly basic ion-exchange resin to obtain optically active amino acids or optically active mandelic acid.

Optically active amino acid-mandelic acid complexes

DL- .alpha.-phenylglycine can be combined with benzene-sulfonic acid, p-ethylbenzenesulfonic acid or m-xylenesulfonic acid to give the salt. The salt of the racemate may be more soluble in a sulfuric acid solution than the salt of the optically active isomer by suitably choosing the concentration of the sulfuric acid solution, and then the optical resolution by fractional crystallization is carried out. The D- or L- .alpha.-phenylglycine sulfonate is easily liberated of the sulfonic acid portion to give optically active D- or L- .alpha.-phenylglycine.

Process for the preparation of optically active .alpha.-phenylglycine

Optically active p-hydroxyphenylglycine is prepared by reacting a racemic compound of a specified p-hydroxyphenylglycine derivative with optically active .alpha.-phenylethylamine to form a corresponding salt, obtaining two types of optically active salts therefrom by fractional crystallization, and obtaining optically active p-hydroxyphenylglycine by decomposition and hydrolysis of at least one of the optically active salts.

Process for the preparation of optically active p-hydroxyphenylglycine

Optically active p-hydroxyphenylglycine is manufactured by inoculating a supersaturated solution of a p-hydroxyphenylglycine sulfonic acid derivative salt comprising a mixture of the two optically active enantiomers of said salt with an optically active enantiomer of the same salt, said mixture being either racemic or else one in which the predominant enantiomer is that of the inoculant. In this manner the enantiomer having the form of the inoculant is selectively crystallized. The selectively crystallized salt is thereafter treated for removal of the sulfonic acid derivative.

Method of manufacturing optically active p-hydroxyphenylglycine

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Tokyo, Japan

Shigeru Aoki