Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: Techniques are provided for optimizing bandwidth in a network. Information describing a network bandwidth capacity of a port extender device is received at a switch. The port extender device is connected to the switch. The port extender device is configured to provide ports for the switch. The network bandwidth capacity of the port extender device is compared to a minimum network bandwidth guarantee threshold. If the switch determines that the network bandwidth capacity of the port extender device is below the minimum network guarantee threshold, the switch sends to the port extender device a message configured to cause the port extender to deactivate one or more links between the port extender device and one or more servers in communication with the port extender device.

Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: Techniques are provided for optimizing bandwidth in a network. Information describing a network bandwidth capacity of a port extender device is received at a switch. The port extender device is connected to the switch. The port extender device is configured to provide ports for the switch. The network bandwidth capacity of the port extender device is compared to a minimum network bandwidth guarantee threshold. If the switch determines that the network bandwidth capacity of the port extender device is below the minimum network guarantee threshold, the switch sends to the port extender device a message configured to cause the port extender to deactivate one or more links between the port extender device and one or more servers in communication with the port extender device.

Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: A system and method for parallel file system traversal using multiple job executors is disclosed. The system includes a pool of job executors, a job queue, and a trigger tracker. An object, representative of a node in the filesystem, is added (i.e., pushed) to the job queue for processing by an job executor. The job queue assigns (i.e., pops) objects to job executors in accordance to a LIFO (Last In First Out) ordering. Then the job executor performs an action such as copy. In one embodiment, the trigger tracker follows the processing of a child nodes to a particular child node. Thus, the filesystem is being traversed by several job executors at the same time.

Abstract: A system and method for parallel file system traversal using multiple job executors is disclosed. The system includes a pool of job executors, a job queue, and a trigger tracker. An object, representative of a node in the filesystem, is added (i.e., pushed) to the job queue for processing by an job executor. The job queue assigns (i.e., pops) objects to job executors in accordance to a LIFO (Last In First Out) ordering. Then the job executor performs an action such as copy. In one embodiment, the trigger tracker follows the processing of a child nodes to a particular child node. Thus, the filesystem is being traversed by several job executors at the same time.

Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: Crystalline solid forms of tigecycline, Form I, Form II, Form III, Form IV, and Form V, compositions comprising these crystalline solid forms, and processes for preparing these crystalline solid forms are described herein.

Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: The invention relates to processes for the preparation of the bicyclic oxazine carboxaldehyde Compound 1: The invention also relates to the use of Compound 1 in the preparation of ?-lactamase inhibitors.

Abstract: This invention relates to crystalline polymorphs of (3S)-N-hydroxy4-({4-[(4-hydroxy-2-butynyl)oxy]phenyl}sulfonyl)-2,2-dimethyl-3-thiomorpholine carboxamide, and preparation and uses thereof.

Abstract: Provided are methods for the preparation of certain substituted pyrrolidine compounds, forms of (2S,4R)-1-(2-aminoacetyl)-4-benzamidopyrrolidine-2-carboxylic acid hydrochloride, and methods for preparing and using these forms.

Abstract: The present invention provides cycloalkylfused indole, benzothiophene, benzofuran, and indene derivatives, and methods for using them to, for example, treat, prevent and/or ameliorate central nervous system diseases by antagonizing 5-HT1A receptors and modulating serotonin levels.

Abstract: The present invention provides improved synthetic methods for the preparation of compounds that modulate proliferation or differentiation in a cell or tissue.

Abstract: The present invention provides cycloalkylfused indole, benzothiophene, benzofuran, and indene derivatives, and methods for using them to, for example, treat, prevent and/or ameliorate central nervous system diseases by antagonizing 5-HT1A receptors and modulating serotonin levels.

Abstract: Crystalline solid forms of tigecycline, Form I, Form II, Form III, Form IV, and Form V, compositions comprising these crystalline solid forms, and processes for preparing these crystalline solid forms are described herein.

Abstract: Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

Abstract: Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

Abstract: Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.