Abstract: A memory block is provided that is shared between two endpoints. This first endpoint is either a host for a virtual machine or the virtual machine. The second endpoint is either the host or another virtual machine. The shared memory block includes a buffer, a post counter, and an acknowledgment counter. The block is employed for communicating data from the first endpoint to the second endpoint. Sending data to the second endpoint includes identifying the buffer as being currently owned by the first endpoint and storing data in the buffer. It is then detected that the acknowledgment counter is equal to the post counter. The post counter is then incremented to signal that data has been stored for receipt by the second endpoint. Receiving the data by the second endpoint includes detecting that the post counter has changed and then incrementing the acknowledgment counter to acknowledge receipt of the data.

Abstract: A memory block is provided that is shared between two endpoints. This first endpoint is either a host for a virtual machine or the virtual machine. The second endpoint is either the host or another virtual machine. The shared memory block includes a buffer, a post counter, and an acknowledgment counter. The block is employed for communicating data from the first endpoint to the second endpoint. Sending data to the second endpoint includes identifying the buffer as being currently owned by the first endpoint and storing data in the buffer. It is then detected that the acknowledgment counter is equal to the post counter. The post counter is then incremented to signal that data has been stored for receipt by the second endpoint. Receiving the data by the second endpoint includes detecting that the post counter has changed and then incrementing the acknowledgment counter to acknowledge receipt of the data.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: Different polymorphs of bromfenac sodium may be prepared and interconverted using crystallization/recrystallization, drying and/or hydration techniques.

Abstract: The present invention relates to a method for the stereospecific synthesis of an enantiomer of a chiral amine, wherein the chiral amine has the formula R.sup.1 CH(NH.sub.2)R.sup.2. R.sup.1 and R.sup.2 are each independently selected from the group consisting of alkyl, aryl and heterocyclic and radicals. This method is particularly useful for stereospecifically synthesizing S-dolaphenine. The method involves contacting a chiral enantiomer of norephedrine with borane, within an aprotic solvent to form a complex for stereospecifically reducing oximes. The complex is then contacted with an oxime, thereby stereospecifically reducing said oxime to form an enantiomer of a chiral amine.

Abstract: The present invention relates to a method for the stereospecific synthesis of an enantiomer of a chiral amine, wherein the chiral amine has the formula R.sup.1 CH(NH.sub.2)R.sup.2. R.sup.1 and R.sup.2 are each independently selected from the group consisting of alkyl, aryl and heterocyclic and radicals. This method is particularly useful for stereospecifically synthesizing S-dolaphenine. The method involves contacting a chiral enantiomer of norephedrine with borane, within an aprotic solvent to form a complex for stereospecifically reducing oximes. The complex is then contacted with an oxime, thereby stereospecifically reducing said oxime to form an enantiomer of a chiral amine.