公开(公告)号：US20160123824A1

公开(公告)日：2016-05-05

申请号：US14412906

申请日：2012-07-09

Applicant: Ji An Wan ,  Kaisheng David Xu

Inventor： Ji An Wan ,  Kaisheng David Xu

IPC: G01L5/28 ,  B25B23/142 ,  F16D66/00

CPC classification number: G01L5/28 ,  B25B23/1427 ,  B66B5/0037 ,  B66B29/00 ,  B66B31/00 ,  F16D66/00 ,  F16D2066/005 ,  G01L5/288

Abstract: A brake torque inspection method to a device having a drive machine and a driven component operatively connected to the drive machine is disclosed. The method comprises applying a brake to the driven component, and using a torque wrench at a shaft of the drive machine to determine the brake torque.

Abstract translation: 公开了一种具有驱动机器和可操作地连接到驱动机器的从动部件的装置的制动转矩检查方法。 该方法包括向驱动部件施加制动器，并且在驱动机器的轴处使用扭矩扳手来确定制动转矩。

公开(公告)号：US20150179595A1

公开(公告)日：2015-06-25

申请号：US14136908

申请日：2013-12-20

Applicant: Mihir Oka ,  Xavier Brun ,  Dingying David Xu ,  Edward Prack ,  Kabirkumar Mirpuri ,  Saikumar Jayaraman

Inventor： Mihir Oka ,  Xavier Brun ,  Dingying David Xu ,  Edward Prack ,  Kabirkumar Mirpuri ,  Saikumar Jayaraman

IPC: H01L23/00 ,  C08L79/04 ,  B23K1/00 ,  C08L77/00 ,  C08K3/22 ,  B23K1/20 ,  C08G69/00 ,  C08K3/36

CPC classification number: H01L24/11 ,  B23K1/0016 ,  B23K1/20 ,  B23K26/361 ,  B23K26/362 ,  B23K2101/42 ,  C08G73/0233 ,  C08K3/22 ,  C08K3/36 ,  C08K2003/2241 ,  C09D179/02 ,  H01L24/05 ,  H01L24/13 ,  H01L2224/0401 ,  H01L2224/05647 ,  H01L2224/1132 ,  H01L2224/11334 ,  H01L2224/1147 ,  H01L2224/1181 ,  H01L2224/11849 ,  H01L2224/119 ,  H01L2224/131 ,  H01L2224/13294 ,  H01L2224/133 ,  H01L2224/13347 ,  H01L2224/1339 ,  H01L2224/16145 ,  H01L2224/16225 ,  H01L2224/81191 ,  H01L2924/10253 ,  H01L2924/12042 ,  H01L2924/00 ,  H01L2924/00014 ,  H01L2924/014 ,  H01L2924/00012 ,  C08L79/04 ,  C08L79/02

Abstract: This disclosure relates generally to generating a solder-on-die using a water-soluble resist, system, and method. Heat may be applied to solder as applied to a hole formed in a water-soluble resist coating, the water-soluble resist coating being on a surface of an initial assembly. The initial assembly may include an electronic component. The surface may be formed, at least in part, by an electrical terminal of the electronic component, the hole being aligned, at least in part, with the electrical terminal. The solder may be reflowed, wherein the solder couples, at least in part, with the electrical terminal.

Abstract translation: 本公开总体上涉及使用水溶性抗蚀剂，系统和方法来生成管芯上的焊料。 当施加到形成在水溶性抗蚀剂涂层中的孔时，可以将热量施加到焊料上，水溶性抗蚀剂涂层在初始组件的表面上。 初始组件可以包括电子部件。 该表面可以至少部分地由电子部件的电端子形成，该孔至少部分地与电端子对准。 焊料可以被回流，其中焊料至少部分地与电端子耦合。

公开(公告)号：US07906677B2

公开(公告)日：2011-03-15

申请号：US12436991

申请日：2009-05-07

Applicant: Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

Inventor： Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

IPC: C07C227/22 ,  C07C209/62

CPC classification number: C07C211/52 ,  C07C211/56 ,  C07C227/22 ,  C07C229/42 ,  C07C233/15 ,  C07C235/16 ,  C07C235/24 ,  C07C2601/16 ,  C07D209/34

Abstract: A process for the production of a compound of Formula I, or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable prodrug ester thereof, comprising cleaving a lactam of formula II wherein the symbols are as defined, with a base; and precursors therefor and processes for the preparation of the precursors. The compounds of Formula I are pharmaceutically active compounds which are selective inhibitors of Cyclooxygenase II.

Abstract translation: 制备式I化合物或其药学上可接受的盐或其药学上可接受的前药酯的方法，其包括用碱定义其中符号如本文所定义的式II的内酰胺; 及其前体和制备前体的方法。 式I的化合物是作为环加氧酶II的选择性抑制剂的药物活性化合物。

公开(公告)号：US20090275758A1

公开(公告)日：2009-11-05

申请号：US12436991

申请日：2009-05-07

Applicant: Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

Inventor： Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

IPC: C07C209/62 ,  C07D209/34 ,  C07C233/07

CPC classification number: C07C211/52 ,  C07C211/56 ,  C07C227/22 ,  C07C229/42 ,  C07C233/15 ,  C07C235/16 ,  C07C235/24 ,  C07C2601/16 ,  C07D209/34

Abstract: A process for the production of a compound of Formula I, or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable prodrug ester thereof, comprising cleaving a lactam of formula II wherein the symbols are as defined, with a base; and precursors therefor and processes for the preparation of the precursors. The compounds of Formula I are pharmaceutically active compounds which are selective inhibitors of Cyclooxygenase II.

Abstract translation: 制备式I化合物或其药学上可接受的盐或其药学上可接受的前药酯的方法，其包括用碱定义其中符号如本文所定义的式II的内酰胺; 及其前体和制备前体的方法。 式I的化合物是作为环加氧酶II的选择性抑制剂的药物活性化合物。

公开(公告)号：US20080249318A1

公开(公告)日：2008-10-09

申请号：US11893481

申请日：2007-08-16

Applicant: Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

Inventor： Murat Acemoglu ,  Thomas Allmendinger ,  John Vincent Calienni ,  Jacques Cercus ,  Olivier Loiseleur ,  Gottfried Sedelmeier ,  David Xu

IPC: C07D209/34 ,  C07C227/22 ,  C07C211/55 ,  C07C233/01

CPC classification number: C07C211/52 ,  C07C211/56 ,  C07C227/22 ,  C07C229/42 ,  C07C233/15 ,  C07C235/16 ,  C07C235/24 ,  C07C2601/16 ,  C07D209/34

Abstract: A process for the production of a compound of Formula I, or a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable prodrug ester thereof, comprising cleaving a lactam of formula II wherein the symbols are as defined, with a base; and precursors therefor and processes for the preparation of the precursors. The compounds of Formula I are pharmaceutically active compounds which are selective inhibitors of Cyclooxygenase II.

Abstract translation: 制备式I化合物或其药学上可接受的盐或其药学上可接受的前药酯的方法，其包括用碱定义其中符号如本文所定义的式II的内酰胺; 及其前体和制备前体的方法。 式I的化合物是作为环加氧酶II的选择性抑制剂的药物活性化合物。

公开(公告)号：US20050069063A1

公开(公告)日：2005-03-31

申请号：US10674730

申请日：2003-09-30

Applicant: Alan Waltho ,  David Xu

Inventor： Alan Waltho ,  David Xu

IPC: H04B1/12 ,  H04B1/52 ,  H04L1/00

CPC classification number: H04B1/525 ,  H04B1/123

Abstract: A method and apparatus are provided for broadband cancellation of interference signals. A signal transmitted on one communication path acts as an interference signal to a receiver on a second communication path in the system. In an embodiment, a signal transmitted from an antenna using one wireless standard, or protocol, acts as an interference signal for another antenna, co-located in the same system, using another wireless standard, or protocol, and operating in the same or nearby frequency bands. A time delay is applied to a signal sampled from the interference signal to provide substantially broadband cancellation of the interference signal. The sampled signal may be attenuated to match the amplitude of the interference signal on the second communication path. Coupling of the sampled signal from one communication path to the other communication path can provide an 180° phase shift to the sampled signal.

Abstract translation: 提供了用于宽带消除干扰信号的方法和装置。 在一个通信路径上发送的信号作为系统中的第二通信路径上的接收机的干扰信号。 在一个实施例中，使用一个无线标准或协议从天线发送的信号用作另一个天线的干扰信号，该另一个天线使用另一无线标准或协议共同位于同一系统中，并在相同或附近操作 频带。 对从干扰信号采样的信号应用时间延迟以提供干扰信号的基本宽带消除。 采样信号可以被衰减以匹配第二通信路径上的干扰信号的幅度。 将采样信号从一个通信路径耦合到另一个通信路径可以对采样信号提供180°的相移。

公开(公告)号：US5801281A

公开(公告)日：1998-09-01

申请号：US968086

申请日：1997-11-12

Applicant: David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

Inventor： David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

IPC: C07C233/00 ,  C07C233/36 ,  C07C303/00 ,  C07C311/18 ,  C07D257/02

CPC classification number: C07C233/36 ,  C07C311/18 ,  C07D257/02

Abstract: An improved process for preparing 1,1'-�1,4-phenylenebis-(methylene)!-bis-1,4,8,11-tetraazacyclotetradecane comprising the selective functionalization of an acyclic tetraamine, and subsequent dimerization and hydrolyzation/tosylation to obtain a 1,4-phenylenebis-methylene bridged hexatosyl acyclic precursor in a first step, the cyclization of said precursor to obtain a hexatosyl cyclam dimer in a second step, and the detosylation of said cyclam dimer in a third step followed by basification to obtain the desired 1,1'-�1,4-phenylenebis-(methylene)!-bis-1,4,8,11-tetraazacyclotetradecane.

Abstract translation: 制备1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷的改进方法，其包括无环四胺的选择性官能化，随后二聚和水解/甲苯磺酰化至 在第一步中获得1,4-亚苯基双 - 亚甲基桥联的六碳酰基非环状前体，在第二步中环化所述前体以获得己糖基环胞二聚体，并在第三步中对所述环化二聚体进行脱甲苯基化，然后碱化得到 所需的1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷。

公开(公告)号：US5756728A

公开(公告)日：1998-05-26

申请号：US777072

申请日：1996-12-30

Applicant: David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

Inventor： David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

IPC: C07C233/00 ,  C07C233/36 ,  C07C303/00 ,  C07C311/18 ,  C07D257/02 ,  C07D259/00 ,  A61K31/395

CPC classification number: C07C233/36 ,  C07C311/18 ,  C07D257/02

Abstract: An improved process for preparing 1,1'-�1,4-phenylenebis-(methylene)!-bis-1,4,8,11-tetraazacyclotetradecane comprising the selective functionalization of an acyclic tetraamine, and subsequent dimerization and hydrolyzation/tosylation to obtain a 1,4-phenylenebis-methylene bridged hexatosyl acyclic precursor in a first step, the cyclization of said precursor to obtain a hexatosyl cyclam dimer in a second step, and the detosylation of said cyclam dimer in a third step followed by basification to obtain the desired 1,1'-�1,4-phenylenebis-(methylene)!-bis-1,4,8,11-tetraazacyclotetradecane.

Abstract translation: 制备1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷的改进方法，其包括无环四胺的选择性官能化，随后二聚和水解/甲苯磺酰化至 在第一步中获得1,4-亚苯基双 - 亚甲基桥联的六碳酰基非环状前体，在第二步中环化所述前体以获得己糖基环胞二聚体，并在第三步中对所述环化二聚体进行脱甲苯基化，然后碱化得到 所需的1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷。

公开(公告)号：US20140119624A1

公开(公告)日：2014-05-01

申请号：US13850846

申请日：2013-03-26

Applicant: Justis P. Ehlers ,  David Xu ,  Peter K. Kaiser ,  William J. Dupps ,  Sunil K. Srivastava

Inventor： Justis P. Ehlers ,  David Xu ,  Peter K. Kaiser ,  William J. Dupps ,  Sunil K. Srivastava

IPC: G06T7/00 ,  G06T7/60

CPC classification number: G06T7/0012 ,  A61B5/0066 ,  G06T7/0016 ,  G06T7/11 ,  G06T7/12 ,  G06T7/162 ,  G06T7/62 ,  G06T17/20 ,  G06T2207/10101 ,  G06T2207/20016 ,  G06T2207/20072 ,  G06T2207/30041

Abstract: Systems and methods are provided for volumetric analysis of pathologies. A segmentation component is configured to determine, for each of a series of images of a region of interest containing a pathological feature, a set of segmentation boundaries within the image representing a cross-section of the pathological feature. A mesh generation component is configured to link the sets of segmentation boundaries from adjacent images in the series of images to generate a polygonal mesh representing a volumetric reconstruction of the pathological feature. A volumetric measurement component is configured to calculate volumetric parameters from the volumetric reconstruction representing the pathological feature. A user interface is configured to provide the calculated volumetric parameters to an associated display.

Abstract translation: 提供系统和方法用于病理学的体积分析。 分割部分被配置为针对包含病理特征的感兴趣区域的一系列图像中的每一个来确定代表病理特征的横截面的图像内的一组分割边界。 网格生成组件被配置为将所述一组图像中的相邻图像的分割边界集合链接以生成表示病理特征的体积重建的多边形网格。 体积测量部件被配置为从表示病理特征的体积重建计算体积参数。 用户界面被配置为将计算的体积参数提供给相关联的显示。

公开(公告)号：US5612478A

公开(公告)日：1997-03-18

申请号：US413582

申请日：1995-03-30

Applicant: David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

Inventor： David Xu ,  Prasad Kapa ,  Oljan Repic ,  Thomas J. Blacklock

IPC: C07C233/00 ,  C07C233/36 ,  C07C303/00 ,  C07C311/18 ,  C07D257/02

CPC classification number: C07C233/36 ,  C07C311/18 ,  C07D257/02

Abstract: An improved process for preparing 1,1'-[1,4-phenylenebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane comprising the selective functionalization of an acyclic tetraamine, and subsequent dimerization and hydrolyzation/tosylation to obtain a 1,4-phenylenebis-methylene bridged hexatosyl acyclic precursor in a first step, the cyclization of said precursor to obtain a hexatosyl cyclam dimer in a second step, and the detosylation of said cyclam dimer in a third step followed by basification to obtain the desired 1,1'-[1,4-phenylenebis-(methylene)]-bis-1,4,8,11-tetraazacyclotetradecane.

Abstract translation: 制备1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷的改进方法，其包括无环四胺的选择性官能化，随后二聚和水解/甲苯磺酰化至 在第一步中获得1,4-亚苯基双 - 亚甲基桥联的六碳酰基非环状前体，在第二步中环化所述前体以获得己糖基环胞二聚体，并在第三步中对所述环化二聚体进行脱甲苯基化，然后碱化得到 所需的1,1' - [1,4-亚苯基双（亚甲基）] - 双-1,4,8,11-四氮杂环十四烷。