Abstract: Disclosed is a force applying device for orthodontic treatment being elastically expandable and configured to generate a restoring force as an orthodontic force for an orthodontic treatment when compressed. The force applying device comprises a first element and a second element capable of moving relative to each other along a first axis. The force applying device for orthodontic treatment is compressed when the first and second elements move towards each other along the first axis. A first arm extends laterally from a first end of the first element away from the second element. A first connecting part of a first connector is fitted over the first arm. A second connecting part of the first connector is to be fitted over a button fixed on a first jaw to connect the first element to the first jaw. Both the first and the second connecting parts are toroidal in shape.

Abstract: The present invention provides a polypropylene-polyphenylene ether-polystyrene ternary alloy, including the following components in parts by weight: 100 parts of a polypropylene and a polyphenylene ether and a polystyrene, wherein the polypropylene accounts for 10% to 60%, the polyphenylene ether accounts for 10% to 60%, and the polystyrene accounts for 5% to 30%; 5 parts to 25 parts of a compatibilizer; and 10 parts to 60 parts of a polyphosphate compound. The polypropylene-polyphenylene ether-polystyrene ternary alloy of the present invention has an advantage of a less smoke release amount during melt.

Abstract: This application is directed to intra-panel communication in a touch display device in which a touch-integrated timing controller (TTCON) is coupled to touch-embedded source drivers (TSDs) via a plurality of forward links and a set of backward links. The forward links include a first subset of display forward links and a second subset of touch forward links. The TSDs are electrically coupled to a display panel including a plurality of display pixels and a plurality of touch sensors. The TTCON sends a display drive signal including display content data and display control data over the display forward links, and sends a touch control signal including an instruction to initiate an operation mode over the touch forward links. Upon receiving the touch control signal, the TSDs identify the instruction to initiate the operation mode, generate touch data accordingly, and return the touch data to the TTCON via the backward links.

Abstract: This application is directed to intra-panel communication in a touch display device in which a touch-integrated timing controller (TTCON) is coupled to touch-embedded source drivers (TSDs) via a plurality of forward links and a set of backward links. The forward links include a first subset of display forward links and a second subset of touch forward links. The TSDs are electrically coupled to a display panel including a plurality of display pixels and a plurality of touch sensors. The TTCON sends a display drive signal including display content data and display control data over the display forward links, and sends a touch control signal including an instruction to initiate an operation mode over the touch forward links. Upon receiving the touch control signal, the TSDs identify the instruction to initiate the operation mode, generate touch data accordingly, and return the touch data to the TTCON via the backward links.

Abstract: Chiral acetyl-protected aminoethyl quinoline (APAQ), pyridine and imazoline ligands are disclosed that enable Pd (II)-catalyzed enantioselective arylation or heteroarylation of ubiquitous prochiral ?-methylene C—H bonds of aliphatic amides offers an alternative disconnection for constructing ?-chiral centers. Systematic tuning of the ligand structure reveals that a six-membered instead of a five-membered chelation of these types of ligands with the Pd(II) is important for accelerating the C(sp3)-H activation thereby achieving enantioselectivity for quinoline and pyridine ligands.

Abstract: Methods, systems, and apparatus, including computer programs encoded on computer storage media, for grouping a plurality of resources into a plurality of cohorts, wherein each of the plurality of resources is associated with a risk level and a benefit level, and resources in each cohort share the same risk level and the same benefit level; obtaining a plurality of provider-level adjustments; constructing an optimization model for determining a resource flow solution; and according to the plurality of cohort-provider-level adjustments, identifying one or more resources in each of the plurality of cohorts that are provided by a first provider to be transferred to a second provider; and automatically sending one or more requests to the first provider and the second provider to transfer the determined one or more first resources from the first provider to the second provider.

Abstract: The invention includes procedures for stereoselective ?-acylation of carboxylic acids having a ?-carbon atom.

Abstract: The invention includes procedures for stereoselective ?-acylation of carboxylic acids having a ?-carbon atom.

Abstract: This invention discloses the first example of palladium(II)-catalyzed ?-C(sp3)-H iodination or arylation of a wide range of ketones by using a commercially available aminooxyacetic acid auxiliary. This L, X-type directing group overcomes the limitation of the transient directing group approach for -?C(sp3)-H functionalization of ketones. Practical advantages of this method include simple installation of the auxiliary without chromatography, exceptional tolerance of a-functional groups, double bonds and triple bonds and rapid access to diverse sterically hindered quaternary centers.

Abstract: We report the design of a catalytic, bifunctional template that binds heterocyclic substrate via reversible coordination instead of covalent linkage, allowing remote site-selective C—H olefination of heterocycles. The two metal centers coordinated to this template play different roles; anchoring substrates to the proximity of catalyst and cleaving the remote C—H bonds respectively. Using this strategy, we demonstrate remote site-selective C—H olefination of heterocyclic substrates which do not have functional group handles for covalently attaching templates. For instance the olefination can be an alkenylation of a 3-phenylpyridine with an acrylate alkyl ester selective for the meta position of the phenyl group with respect to the pyridine, or can be an alkenylation of a quinoline with an acrylate alkyl ester selective for the 5-position of the quinoline.

Abstract: Pd(II)-catalyzed g-G(sp3)-H arylation or heteroarylation of primary amines is realized by using 2-hydroxynicotinaldehyde as a catalytic transient directing group. Importantly, the catalyst and the directing group loading can be lowered to 2% and 4% respectively, thus demonstrating high efficiency of this newly designed transient directing group. Heterocyclic aryl iodides are also compatible with this reaction. Furthermore, swift synthesis of 1,2,3,4-tetrahydronaphthyridine derivatives is accomplished using this reaction.

Abstract: This invention discloses the first example of palladium(II)-catalyzed ?-C(sp3)-H iodination or arylation of a wide range of ketones by using a commercially available aminooxyacetic acid auxiliary. This L, X-type directing group overcomes the limitation of the transient directing group approach for -?C(sp3)-H functionalization of ketones. Practical advantages of this method include simple installation of the auxiliary without chromatography, exceptional tolerance of a-functional groups, double bonds and triple bonds and rapid access to diverse sterically hindered quaternary centers.

Abstract: A class of mono-protected 3-amino-2-hydroxypyridine (MPAHP) ligands that enable the meta-C—H arylation of anilines, phenols, phenylacetic acids, and biologically relevant heterocyclic compounds using norbornene as a transient mediator is disclosed, such as in the formation of a reaction product of Formula IA: The applicability of this meta-arylation methodology in the pharmaceutical industry is illustrated for heteroaryl substrates and heteroaryl iodide coupling partners, a feat made possible by using the MPAHP ligand. The enabling nature of MPAHP ligands to achieve other meta-C—H functionalization processes is also illustrated by the development of a meta-C—H amination reaction and a meta-C—H alkynylation reaction.

Abstract: We report the design of a catalytic, bifunctional template that binds heterocyclic substrate via reversible coordination instead of covalent linkage, allowing remote site-selective C—H olefination of heterocycles. The two metal centers coordinated to this template play different roles; anchoring substrates to the proximity of catalyst and cleaving the remote C—H bonds respectively. Using this strategy, we demonstrate remote site-selective C—H olefination of heterocyclic substrates which do not have functional group handles for covalently attaching templates. For instance the olefination can be an alkenylation of a 3-phenylpyridine with an acrylate alkyl ester selective for the meta position of the phenyl group with respect to the pyridine, or can be an alkenylation of a quinoline with an acrylate alkyl ester selective for the 5-position of the quinoline.

Abstract: An alternative approach to formation of a C—C bond at a meta-position of an aromatic compound is disclosed that employs an ethylenically unsaturated bicyclic compound as a transient mediator to achieve meta-selective C—H activation with a simple and common ortho-directing group. The use of a pyridine-based ligand assists in relaying the palladium catalyst to the meta-position by the unsaturated bicyclic compound following initial ortho-C—H activation.

Abstract: Disclosed are antibodies thereof that bind to coagulation factor XI (FXI) and/or its activated form factor XIa (FXIa), or to fragments of FXI and/or FXIa, and compositions containing the antibodies. Also disclosed are methods of preparing the antibodies and use of the antibodies for treating and/or preventing coagulation associated conditions such as thrombosis and complications or conditions associated with thrombosis.

Abstract: The vacuum electro-spray ion source comprises a hollow capillary, a vacuum cavity, a gas inlet pipe, a gas supply device and an adjusting device, wherein a first end of the hollow capillary is a sampling port, and a second end is used as a spray nozzle for vacuum electro-sprays and stretches into the vacuum cavity; the air pressure in the vacuum cavity is ranged from 10 to 200 Pa; one end of the gas inlet pipe stretches into the vacuum cavity, and the other end is connected with the gas supply device; and the adjusting device is configured for adjusting the gas inlet pipe to allow the gas to flow therein intermittently. The ion source may achieve electro-spray ionization in the vacuum environment, so that losses during ion transmission may be reduced to improve the signal intensity and detection limit during detection.

Abstract: Chiral acetyl-protected aminoethyl quinoline (APAQ), pyridine and imazoline ligands are disclosed that enable Pd (II)-catalyzed enantioselective arylation or heteroarylation of ubiquitous prochiral ?-methylene C—H bonds of aliphatic amides offers an alternative disconnection for constructing ?-chiral centers. Systematic tuning of the ligand structure reveals that a six-membered instead of a five-membered chelation of these types of ligands with the Pd(II) is important for accelerating the C(sp3)-H activation thereby achieving enantioselectivity for quinoline and pyridine ligands.

Abstract: Pd(II)-catalyzed g-G(sp3)-H arylation or heteroarylation of primary amines is realized by using 2-hydroxynicotinaldehyde as a catalytic transient directing group. Importantly, the catalyst and the directing group loading can be lowered to 2% and 4% respectively, thus demonstrating high efficiency of this newly designed transient directing group. Heterocyclic aryl iodides are also compatible with this reaction. Furthermore, swift synthesis of 1,2,3,4-tetrahydronaphthyridine derivatives is accomplished using this reaction.

Abstract: A class of mono-protected 3-amino-2-hydroxypyridine (MPAHP) ligands that enable the meta-C—H arylation of anilines, phenols, phenylacetic acids, and biologically relevant heterocyclic compounds using norbornene as a transient mediator is disclosed. The applicability of this meta-arylation methodology in the pharmaceutical industry is illustrated for heteroaryl substrates and heteroaryl iodide coupling partners, a feat made possible by using the MPAHP ligand. The enabling nature of MPAHP ligands to achieve other meta-C—H functionalization processes is also illustrated by the development of a meta-C—H amination reaction and a meta-C—H alkynylation reaction.