Abstract: A method includes entering a communication extension mode. After entering the communication extension mode, the method includes outputting via a network, to at least a first device of a first partition and a second device of a second different partition, a first beacon signal of a first communication extension mode frame. The first beacon signal can include a first indication of one slot of the first communication extension mode frame to be output after the first beacon signal and corresponding to a first communication protocol and a second indication of another slot of the first communication extension mode frame to be output after the first beacon signal and corresponding to a second different communication protocol. After outputting the first beacon signal, the method includes using the one slot of the first communication extension mode frame, corresponding to the first communication protocol, to transmit data from the first device of the first partition.

Abstract: The present invention relates to process of enrichment of Boron isotopes by ion exchange chromatography by “Auto Cut” system using continuous Ion Exchange Chromatography. The process comprises development of borate band in the ion exchange chromatographic column; eluting said band without any regeneration in a manner where said ion exchange chromatographic columns comprises 3-9 chromatographic columns in groups of three columns each and connected in series with silicon tubes; and wherein said eluting agent is provided to first column of each said group of three columns; and wherein said enriched boron isotopes are obtained upto 90%.

Abstract: The invention disclosed novel triterpene derivatives of azadirachtin of the formulae 2 to 11 of the drawings and a process for isolating new triterpene derivatives of azadirachtin from the various parts of the neem plant(Azadirachta indica A-Juss), which process comprises grinding the parts of the neem plant to get a powder, extracting the powder with a binary immiscible solvent consisting of one polar and another non-polar solvent in a ratio of 1:2 to obtain an extract, filtering the extract to get a filtrate having two layers, one layer containing lipids and the other layer containing the new triterpene derivatives of azadirachtin and water soluble constituents including sugars, separating the layers by known methods, concentrating the layer containing the new triterpenes of the formulae 2-11 including derviatives of azadirachtin and water soluble salts, treating the resultant concentrate with a polar solvent and if necessary, warm the concentrate having the solvent, and filtering/decanting the resultant so

Abstract: The invention discloses novel triterpene derivatives of azadirachtin of the formulae 2 to 11 of the drawings and a process for isolating new triterpene derivatives of azadirachtin from the various parts of the neem plant(Azadirachta indica A-Juss), which process comprises grinding the parts of the neem plant to get a powder, extracting the powder with a binary immiscible solvent consisting of one polar and another non-polar solvent in a ratio of 1:2 to obtain an extract, filtering the extract to get a filtrate having two layers, one layer containing lipids and the other layer containing the new triterpene derivatives of azadirachtin and water soluble constituents including sugars, separating the layers by known methods, concentrating the layer containing the new triterpenes of the formulae 2-11 including derivatives of azadirachtin and water soluble salts, treating the resultant concentrate with a polar solvent and if necessary, warm the concentrate having the solvent, and filtering/decanting the resultant so

Abstract: The invention resides in a novel photochemical process for the production of .alpha.-aryl propionic acids by the subjection of a solution in an organic solvent of the corresponding .alpha.-haloaryl alkyl ketones to irradiation with light having a wavelength of from 200 to 800 nm, preferably in the presence of a suitable acid scavenger for the neutralization of any hydrohalogen acid generated during the reaction.

Abstract: Codeine is prepared by reacting morphine with trimethyl phenyl ammonium chloride in the presence of an alkali metal carbonate and a hydrocarbon solvent at a temperature of from 40.degree. to 120.degree. C. Codeine is recovered from the reaction mixture. Codeine is useful as an analgesic and antitussive drug.