Patent classifications
C07C213/10
Process for the preparation of l-Norepinephrine bitartrate monohydrate having high enantiomeric purity
The present invention, discloses optically pure compounds of l-Norepinephrine and its acid addition salts and hydrates and process for the preparation thereof. Specifically, the present invention discloses optically pure compounds of l-Norepinephrine bitartrate, its process of preparation and pharmaceutical compositions comprising the same.
CRYSTALLINE FORMS OF (-)-(1R,2R)-3-(3-DIMETHYLAMINO-1-ETHYL-2-METHYLPROPYL)-PHENOL HYDROCHLORIDE
A hitherto unknown crystalline form of ()-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride, pharmaceutical compositions containing the new crystalline form, methods of producing the new crystalline form, and a related method of use including treatment of, e.g., pain and/or urinary incontinence.
CRYSTALLINE FORMS OF (-)-(1R,2R)-3-(3-DIMETHYLAMINO-1-ETHYL-2-METHYLPROPYL)-PHENOL HYDROCHLORIDE
A hitherto unknown crystalline form of ()-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride, pharmaceutical compositions containing the new crystalline form, methods of producing the new crystalline form, and a related method of use including treatment of, e.g., pain and/or urinary incontinence.
POLYMORPHIC FORMS OF RAD1901-2HCL
Various polymorphic forms of RAD1901-2HCl, including three crystalline and amorphous forms, are prepared and characterized. Uses of the various polymorphic forms of RAD1901-2HCl for cancer treatment are also disclosed.
POLYMORPHIC FORMS OF RAD1901-2HCL
Various polymorphic forms of RAD1901-2HCl, including three crystalline and amorphous forms, are prepared and characterized. Uses of the various polymorphic forms of RAD1901-2HCl for cancer treatment are also disclosed.
ENANTIOSELECTIVE DESTRUCTION OF CHIRAL MOLECULES
Methods and devices are disclosed for selective photo-destruction of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. Methods and devices are disclosed for selective enrichment of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. The nanostructures support optical frequency electric resonances and optical frequency magnetic resonances.
ENANTIOSELECTIVE DESTRUCTION OF CHIRAL MOLECULES
Methods and devices are disclosed for selective photo-destruction of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. Methods and devices are disclosed for selective enrichment of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. The nanostructures support optical frequency electric resonances and optical frequency magnetic resonances.
ENANTIOSELECTIVE DESTRUCTION OF CHIRAL MOLECULES
Methods and devices are disclosed for selective photo-destruction of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. Methods and devices are disclosed for selective enrichment of one chiral enantiomer of a compound using nanostructures by enhancing differential absorption of circularly polarized light by the one chiral enantiomer. The nanostructures support optical frequency electric resonances and optical frequency magnetic resonances.
Organic reactions carried out in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose
The present invention relates to a method of carrying out an organic reaction in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose.
Organic reactions carried out in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose
The present invention relates to a method of carrying out an organic reaction in aqueous solution in the presence of a hydroxyalkyl(alkyl)cellulose or an alkylcellulose.