| Patent application number | Description | Published |
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| 20090307490 | ELECTRONIC DATA COMMUNICATION SYSTEM - There is described an electronic data communication system in which encrypted mail messages for a recipient are sent in two parts: message data encrypted by a symmetric encryption algorithm using a session key and session key data encrypted by an asymmetric encryption algorithm using a public key associated with the recipient. If the recipient uses a webmail service to access the encrypted electronic mail message, the encrypted session key data is sent to a trusted third party server which has access to the private key of the user. The trusted third party server decrypts the encrypted session key using the private key of the user, and then sends the decrypted session key to a remote network device for decryption of the encrypted message. In this way, although the trusted third party has access to the private key of the user, the trusted third party does not have access to any decrypted message. In another aspect, in order to digitally sign a message, the sender applies a hash function to the message to generate a hash value, and then sends the hash value to the trusted third party server where it is encrypted using the private key associated with the sender in order to generate the digital signature, which is then returned to the sender. | 12-10-2009 |
| 20100046757 | Electronic Data Communication System - There is described an electronic mail messaging system in which a plurality of user computers are connected to a mail registration server via the Internet. The mail registration server stores plural sets of decryption data, each set being required to decrypt a corresponding encrypted electronic mail message. Following receipt of an encrypted electronic mail message, a user computer communicates with the mailed registration server to effect decryption of the encrypted electronic mail message using the corresponding decryption data stored by the mail registration server. In this way, the accessing of the electronic mail message can be monitored by the mail registration server. | 02-25-2010 |
| 20100228973 | ELECTRONIC DATA COMMUNICATION SYSTEM - There is described a key server which is connected to a local area network, and an encryption authority transfers private keys for clients of the local area network to the key server. In an embodiment, the key server encrypts outgoing emails using public keys for the recipients and decrypts internal emails using private keys for the recipients. In another embodiment, the clients of the local area network download their respective private keys from the key server so that encryption operations may be performed by client software. | 09-09-2010 |
| Patent application number | Description | Published |
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| 20090069582 | METHOD FOR MANUFACTURE OF ESCITALOPRAM - This patent discloses a method for resolution of 4-[4-(dimethylamino)-1-(4′-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)-benzonitrile as a racemic or non-racemic enantiomer mixture into its isolated enantiomers, said method comprising the step of fractionally crystallizing 4-[4-(dimethylamino)-1-(4′-fluoro-phenyl)-1-hydroxybutyl]-3-(hydroxymethyl)-benzonitrile as a salt with the (+)—(S,S)— or (−)—(R,R)-enantiomer of O,O′-di-p-toluoyl-tartaric acid in a solvent system comprising 1-propanol, ethanol or acetonitrile. | 03-12-2009 |
| 20090247772 | Method for the Preparation of Escitalopram - The invention relates to intermediates and the use thereof in a method for the preparation of escitalopram: | 10-01-2009 |
| 20110046218 | CRYSTALLINE BASE OF ESCITALOPRAM AND ORODISPERSIBLE TABLETS COMPRISING ESCITALOPRAM BASE - The present invention relates to the crystalline base of the well known antidepressant drug escitalopram, S-1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile, formulations of said base, a process for the preparation of purified salts of escitalopram, such as the oxalate, using the base, the salts obtained by said process and formulations containing such salts, and a process for the preparation of purified escitalopram free base or salts of escitalopram, such as the oxalate, using the hydrobromide, the salts obtained by said process and formulations containing such salts. Finally the present invention relates to an orodispersible tablet having a hardness of at least 22 N and an oral-disintegration time of less than 120 s and comprising an active pharmaceutical ingredient adsorbed onto a water soluble filler wherein the active pharmaceutical ingredient has a melting point in the range of 40-100° C., as well as a method for making such an orodispersible tablet. | 02-24-2011 |
| 20110065937 | METHOD FOR THE SEPARATION OF INTERMEDIATES WHICH MAY BE USED FOR THE PREPARATION OF ESCITALOPRAM - The present invention relates to a novel method for the preparation of diol intermediates having the formula (II) and/or the opposite enantiomer of an acylated diol having the formula (IV) useful for the preparation of escitalopram involving selective enzymatic acylation or deacylation. | 03-17-2011 |
