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71. 发明授权

US07632379B2 Plasma source and plasma processing apparatus 有权
标题翻译：等离子体源和等离子体处理装置
公开(公告)号：US07632379B2
公开(公告)日：2009-12-15
申请号：US10558692
申请日：2004-05-28
申请人： Toshio Goto , Masaru Hori , Nobuo Ishii , Shoji Den
发明人： Toshio Goto , Masaru Hori , Nobuo Ishii , Shoji Den
IPC分类号： C23F1/00 , H01L21/306 , C23C16/00
CPC分类号： B82Y30/00 , B82Y40/00 , C01B32/162 , H01J37/32009 , H01J37/32596
摘要： A plasma source (1) is composed of a chamber (2) to which a gas should be supplied and a hollow cathode electrode member (4) which is arranged on the gas flow-out side of the chamber (2) and has a plurality of electrode holes (3) through which the gas can flow. In such a plasma source (1), microcathode plasma discharge can be performed in the electrode holes (3) of the hollow cathode electrode member (4).
摘要翻译：等离子体源（1）由供应气体的室（2）和设置在室（2）的气体流出侧的中空阴极电极构件（4）构成，并且具有多个的气体可以流过的电极孔（3）。在这种等离子体源（1）中，可以在中空阴极电极部件（4）的电极孔（3）中进行微阴极等离子体放电。

72. 发明授权

US06358886B1 6-Substituted 2,4-diamino-1,3,5-triazine derivatives having at least two asymmetrically substituted carbon atoms, the production thereof, and their use as herbicides 失效
标题翻译：具有至少两个不对称取代的碳原子的6-取代的2,4-二氨基-1,3,5-三嗪衍生物，其制备及其作为除草剂的用途
公开(公告)号：US06358886B1
公开(公告)日：2002-03-19
申请号：US09623612
申请日：2000-11-03
申请人： Hans-Jochem Riebel , Stefan Lehr , Katharina Voigt , Markus Dollinger , Mark Wilhelm Drewes , Ingo Wetcholowsky , Randy Allen Myers , Yukiyoshi Watanabe , Toshio Goto
发明人： Hans-Jochem Riebel , Stefan Lehr , Katharina Voigt , Markus Dollinger , Mark Wilhelm Drewes , Ingo Wetcholowsky , Randy Allen Myers , Yukiyoshi Watanabe , Toshio Goto
IPC分类号： C07D25118
CPC分类号： C07D405/12 , A01N43/68 , C07D251/48 , C07D409/12
摘要： The invention relates to novel substituted optically active aminotriazines having at least two asymmetrically substituted carbon atoms of the formula (I), in which A represents a single bond or represents in each case straight-chain or branched alkanediyl or oxaalkanediyl having in each case up to 6 carbon atoms, Z represents certain carbocyclic or heterocyclic radicals and the substituents R1, R2, R3, R4 and Y are as defined in the description, with the proviso that in each individual case R2, R3 and Y are different from one another and that the substituents at the two carbon atoms to which R2 and R3 or R4 are attached are configured as follows: (a) R configuration at the carbon atom to which R2 and R3 are attached and R configuration at the carbon atom to which R4 is attached (“R,R-diastereomers”), (b) R configuration at the carbon atom to which R2 and R3 are attached and S configuration at the carbon atom to which R4 is attached (“R,S-diastereomers”), (c) S configuration at the carbon atom to which R2 and R3 are attached and R configuration at the carbon atom to which R4 is attached (“S,R-diastereomers”), (d) S configuration at the carbon atom to which R2 and R3 are attached and S configuration at the carbon atom to which R4 is attached (“S,S-diastereomers”), (e) R configuration at the carbon atom to which R2 and R3 are attached and racemic configuration at the carbon atom to which R4 is attached (“R,racdiastereomers”), (f) S configuration at the carbon atom to which R2 and R3 are attached and racemic configuration at the carbon atom to which R4 is attached (“S,rac-diastereomers”), and to a process for preparing the compounds of the formula (I) and to their use as herbicides.
摘要翻译：本发明涉及具有式（I）的至少两个不对称取代的碳原子的新的取代的光学活性氨基三嗪，其中A表示单键或表示在每种情况下为直链或支链烷二基或氧杂烷二基，在每种情况下最多为6 碳原子，Z表示某些碳环或杂环基团，并且取代基R 1，R 2，R 3，R 4和Y如说明书中所定义，条件是在各个别情况下，R 2，R 3和Y彼此不同， R2和R3或R4连接的两个碳原子上的取代基配置如下：（a）R 2和R 3连接的碳原子上的R构型，R 4连接的碳原子上的R构型（“ R，R非对映异构体“），（b）R 2和R 3连接的碳原子上的R构型，R 4连接的碳原子上的S构型（”R，S-非对映异构体“），（c）S 配置在碳ato m与R 2相连的碳原子上的R构型（“S，R-非对映异构体”），（d）在R2和R3所连接的碳原子上的S构型， R 4连接的碳原子（“S，S-非对映异构体”），（e）R 2和R 3所连接的碳原子上的R构型，R 4连接的碳原子上的外消旋构型（“R” 外消旋异构体“），（f）R 2和R 3所连接的碳原子上的S构型以及与R4连接的碳原子上的外消旋构型（”S，外消旋 - 非对映体“），以及制备该化合物的方法的式（I）和它们作为除草剂的用途。

73. 发明授权

US06282214B1 Wavelength multiplexing light source 失效
标题翻译：波长复用光源
公开(公告)号：US06282214B1
公开(公告)日：2001-08-28
申请号：US09262331
申请日：1999-03-04
申请人： Ryosuke Goto , Kazuo Yamane , Toshio Goto , Masakazu Mori
发明人： Ryosuke Goto , Kazuo Yamane , Toshio Goto , Masakazu Mori
IPC分类号： H01S310
CPC分类号： H04B10/506 , H01S5/4006 , H01S5/4025 , H01S5/4087
摘要： In a wavelength multiplexing light source used in an optical wavelength division multiplexing (WDM) transmission system and the like, at least three semiconductor lasers of single longitudinal mode have oscillation frequencies outside of their pull-in range at a normal injection locking without a modulation side band, an output light of a first semiconductor laser is injected in one way into a second semiconductor laser having an oscillation frequency adjacent to that of the first o semiconductor laser through a first one-way optical injection means to generate a modulation side band. The output light of the second semiconductor laser is then injected in one way into a third semiconductor laser having an oscillation frequency adjacent to that of the second semiconductor laser through a second one-way optical injection means to generate the modulation side band for an injection locking.
摘要翻译：在光波分复用（WDM）传输系统等中使用的波长复用光源中，在纵向模式的至少三个半导体激光器的正常注入锁定下，在没有调制侧的情况下，具有超出其拉入范围的振荡频率第一半导体激光器的输出光通过第一单向光注入装置以一种方式注入具有与第一半导体激光器的振荡频率相邻的振荡频率的第二半导体激光器中，以产生调制边带。然后，第二半导体激光器的输出光通过第二单向光注入装置以一种方式注入具有与第二半导体激光器相邻的振荡频率的第三半导体激光器，以产生用于注入锁定的调制侧带。

74. 发明授权

US06222754B1 Digital signal recording/reproducing method 失效
公开(公告)号：US06222754B1
公开(公告)日：2001-04-24
申请号：US09270510
申请日：1999-03-17
申请人： Toshio Goto , Takashi Yamaji
发明人： Toshio Goto , Takashi Yamaji
IPC分类号： G11C1304
CPC分类号： G11B7/0065 , G11C13/042
摘要： Digital signal sequences to be recorded in predetermined unitary recording areas are transformed into blocks, a plurality of bit data carrying all digit levels to be read and determined upon reproduction are included in the resultant blocks, and sequences of the data blocks are recorded in the recording medium in the unitary recording areas. Upon reproduction, the blocks of the read signals obtained from a recording medium are recognized, a threshold value is determined for each block on the basis of the values of read signals corresponding to bit data carrying all digit levels to be read and determined, and each digit level of bit data in the read signal are read and determined on the basis of the threshold values.

75. 发明授权

US06201005B1 Method for inhibiting lymphokine production 失效
标题翻译：抑制淋巴细胞生成的方法
公开(公告)号：US06201005B1
公开(公告)日：2001-03-13
申请号：US09411630
申请日：1999-10-01
申请人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
发明人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
IPC分类号： A01N4338
CPC分类号： C07D498/18 , C07H19/01 , C12P17/188 , C12P19/44 , C12R1/465 , C12R1/55 , Y02P20/55 , Y10S435/886 , Y10S435/898
摘要： This invention relates to tricyclo compounds useful for treatment and prevention of resistance by transplantation, graft-versus-host diseases by medulla ossium transplantation autoimmune diseases, infectious diseases, and the like, which can be represented by the following formula: to a process for their production, to a pharmaceutical composition containing the same and to a use thereof.
摘要翻译：本发明涉及可用于治疗和预防移植抵抗力的三环化合物，通过髓质骨移植自身免疫性疾病，传染病等的移植物抗宿主病，其可以由下式表示：制备成含有该组合物的药物组合物及其用途。

76. 发明授权

US5668087A Herbicidal 1-alkenyltetrazolinones 失效
标题翻译：除草剂1-烯基四唑啉酮
公开(公告)号：US5668087A
公开(公告)日：1997-09-16
申请号：US616674
申请日：1996-03-15
申请人： Toshio Goto , Yoshinori Kitagawa , Seishi Ito , Katsuhiko Shibuya , Kazuhiro Ukawa , Yoshiko Kyo , Natsuko Minegishi
发明人： Toshio Goto , Yoshinori Kitagawa , Seishi Ito , Katsuhiko Shibuya , Kazuhiro Ukawa , Yoshiko Kyo , Natsuko Minegishi
IPC分类号： C07D401/06 , A01N47/38 , C07D257/04 , C07D403/06 , A01N43/713
CPC分类号： C07D257/04 , A01N47/38
摘要： Herbicidal 1-alkenyltetrazolinones of the formula: ##STR1## wherein R.sup.1 represents the group: ##STR2## or the group: ##STR3## R.sup.2 and R.sup.3, independently of one another, represent C.sub.1-6 alkyl, C.sub.3-7 cycloalkyl which may optionally be substited by methyl, C.sub.2-4 alkenyl, C.sub.2-5 alkynyl, phenyl which may optionally be substituted or aralkyl which may optionally be substituted, orR.sup.2 and R.sup.3 may optionally form, together with the N-atom to which they are bonded, a heterocyclic ring which may optionally be substituted, and novel intermediates therefor.
摘要翻译：下式的除草1-烯基四唑啉酮：彼此独立地表示C 1-6烷基，可以任选地被甲基，C 2-4烯基，C 2-5炔基，可任选被取代的苯基或任选被取代的芳基烷基的C 3-7环烷基可以任选地被取代，或者R 2和R 3可以任选地与它们所键合的N-原子一起形成可以任选被取代的杂环，以及其新颖的中间体。

77. 发明授权

US5624842A Strain of Streptomyces for the production of tricyclo compounds 失效
标题翻译：用于生产三环化合物的链霉菌菌株
公开(公告)号：US5624842A
公开(公告)日：1997-04-29
申请号：US450412
申请日：1995-05-25
申请人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
发明人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
IPC分类号： A01N43/38 , A61K31/00 , A61K31/33 , A61K31/40 , A61K31/407 , A61K31/435 , A61K31/4353 , A61K31/436 , A61K31/445 , A61K31/4465 , A61K31/4523 , A61K31/453 , A61K31/4745 , A61P31/00 , A61P31/04 , A61P37/00 , A61P37/06 , C07D491/14 , C07D498/04 , C07D498/14 , C07D498/18 , C07D519/00 , C07H19/01 , C12N1/20 , C12P17/16 , C12P17/18 , C12P19/44 , C12R1/465 , C12R1/55
CPC分类号： C07D498/18 , C07H19/01 , C12P17/188 , C12P19/44 , C12R1/465 , C12R1/55 , Y02P20/55 , Y10S435/886 , Y10S435/898
摘要： This invention relates to tricyclo compounds useful for treatment and prevention of resistance by transplantation, graft-versus-host diseases by medulla ossium transplantation, autoimmune diseases, infectious diseases, and the like, which can be represented by the following formula: ##STR1## to a process for their production, to a pharmaceutical composition containing the same and to a use thereof.
摘要翻译：本发明涉及可用于治疗和预防移植抵抗的三环类化合物，通过髓质移植移植物抗宿主病，自身免疫性疾病，感染性疾病等，其可以由下式表示：（ I）涉及其制备方法，含有该方法的药物组合物及其用途。

78. 发明授权

US5496727A Tricyclo compounds, a process for their production and a pharmaceutical composition containing the same 失效
公开(公告)号：US5496727A
公开(公告)日：1996-03-05
申请号：US450639
申请日：1995-05-25
申请人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
发明人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
IPC分类号： A01N43/38 , A61K31/00 , A61K31/33 , A61K31/40 , A61K31/407 , A61K31/435 , A61K31/4353 , A61K31/436 , A61K31/445 , A61K31/4465 , A61K31/4523 , A61K31/453 , A61K31/4745 , A61P31/00 , A61P31/04 , A61P37/00 , A61P37/06 , C07D491/14 , C07D498/04 , C07D498/14 , C07D498/18 , C07D519/00 , C07H19/01 , C12N1/20 , C12P17/16 , C12P17/18 , C12P19/44 , C12R1/465 , C12R1/55
CPC分类号： C07D498/18 , C07H19/01 , C12P17/188 , C12P19/44 , C12R1/465 , C12R1/55 , Y02P20/55 , Y10S435/886 , Y10S435/898
摘要： This invention relates to tricyclo compounds useful for treatment and prevention of resistance by transplantation, graft-versus-host diseases by medulla ossium transplantation, autoimmune diseases, infectious diseases, and the like, which can be represented by the following formula: ##STR1## to a process for their production, to a pharmaceutical composition containing the same and to a use thereof.

79. 发明授权

US5110811A Tricyclo compounds, a process for their production and a pharmaceutical composition containing the same 失效
标题翻译：三肽化合物，其生产方法和含有它们的药物组合物
公开(公告)号：US5110811A
公开(公告)日：1992-05-05
申请号：US491205
申请日：1990-03-09
申请人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
发明人： Masakuni Okuhara , Hirokazu Tanaka , Toshio Goto , Tohru Kino , Hiroshi Hatanaka
IPC分类号： A01N43/38 , A61K31/00 , A61K31/33 , A61K31/40 , A61K31/407 , A61K31/435 , A61K31/4353 , A61K31/436 , A61K31/445 , A61K31/4465 , A61K31/4523 , A61K31/453 , A61K31/4745 , A61P31/00 , A61P31/04 , A61P37/00 , A61P37/06 , C07D491/14 , C07D498/04 , C07D498/14 , C07D498/18 , C07D519/00 , C07H19/01 , C12N1/20 , C12P17/16 , C12P17/18 , C12P19/44 , C12R1/465 , C12R1/55
CPC分类号： C07D498/18 , C07H19/01 , C12P17/188 , C12P19/44 , C12R1/465 , C12R1/55 , Y02P20/55 , Y10S435/886 , Y10S435/898
摘要： This invention relates to tricyclo compounds useful for treatment and prevention of resistance by transplantation, graft-versus-host diseases by medulla ossium transplantation, autoimmune diseases, infectious diseases, and the like, which can be represented by the following formula: ##STR1## to a process for their production, to a pharmaceutical composition containing the same and to a use thereof.

80. 发明授权

US4747865A Substituted phenoxyalkanecarboxylic acid esters 失效
标题翻译：取代的苯氧亚硬脂酸酯
公开(公告)号：US4747865A
公开(公告)日：1988-05-31
申请号：US934774
申请日：1986-11-25
申请人： Kozo Shiokawa , Koichi Moriya , Toshio Goto , Atsumi Kamochi , Seishi Ito , Mitsugu Horita
发明人： Kozo Shiokawa , Koichi Moriya , Toshio Goto , Atsumi Kamochi , Seishi Ito , Mitsugu Horita
IPC分类号： A01N43/76 , A01N43/78 , C07D263/58 , C07D277/68
CPC分类号： C07D263/58 , A01N43/76 , C07D277/68
摘要： Novel substituted phenoxyalkanecarboxylic acid esters of the formula ##STR1## in which R.sup.1 and R.sup.2, independently of one another, are a hydrogen atom, a halogen atom, a lower alkyl group or a nitro group, orR.sup.1 and R.sup.2, together with the benzene ring to which they are bonded, are a naphthalene ring,R.sup.3 and R.sup.4, independently of one another, are a hydrogen atom or a methyl group,n is 1 or 2,m is 0 or 1,X is an oxygen atom, a sulfur atom, a sulfonyl group or a group of the formula ##STR2## in which R.sup.6 is a lower alkyl group, R.sup.5 is a hydrogen atom or a halogen atom, andY is an oxygen atom or a sulfur atom, and the use of the new compounds as herbicides.
摘要翻译：式（Ⅰ）的新型取代的苯氧亚硬脂酸酯：其中R 1和R 2彼此独立地是氢原子，卤原子，低级烷基或硝基，或者R 1和R 2 与它们所键合的苯环一起为萘环，R 3和R 4彼此独立地为氢原子或甲基，n为1或2，m为0或1，X为氧原子，硫原子，磺酰基或式“IMAGE”的基团，其中R6是低级烷基，R5是氢原子或卤素原子，Y是氧原子或硫原子，和使用新化合物作为除草剂。

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