Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Dihydrocodeinone"'
Autor:
Damien Maurel, Christian Gentzsch, Sébastien Granier, Kerstin Seier, Harald Hübner, Yann Lanoiselée, Zsombor Koszegi, Davide Calebiro, Peter Gmeiner, Michael Decker, Marie-Lise Jobin, Antonios Drakopoulos, Remy Sounier
Publikováno v:
Angewandte Chemie (International Ed. in English)
μ‐Opioid receptors (μ‐ORs) play a critical role in the modulation of pain and mediate the effects of the most powerful analgesic drugs. Despite extensive efforts, it remains insufficiently understood how μ‐ORs produce specific effects in liv
Autor:
Helena Hulkova, Monika Arenbergerova, J. Sikora, O. Trhlikova, Spyridon Gkalpakiotis, P. Arenberger, Eva Sticova
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVReferences. 34(1)
Background 'Braun' is an illegal injectable dihydrocodeinone-enriched drug mixture of semi-synthetic opioids. It is prepared by palladium-catalysed hydrogenation from codeine-containing tablets. Objective We aimed to characterize the dermatologic con
Autor:
Zsombor Koszegi, Marie-Lise Jobin, Harald Hübner, Sébastien Granier, Antonios Drakopoulos, Yann Lanoiselée, Kerstin Seier, Davide Calebiro, Damien Maurel, Peter Gmeiner, Remy Sounier, Christian Gentzsch, Michael Decker
Publikováno v:
Angewandte Chemie. 132:6348-6348
Autor:
Michael Decker, Sébastien Granier, Kerstin Seier, Davide Calebiro, Christian Gentzsch, Remy Sounier, Damien Maurel, Marie-Lise Jobin, Antonios Drakopoulos, Harald Hübner, Zsombor Koszegi, Yann Lanoiselée, Peter Gmeiner
Publikováno v:
Angewandte Chemie International Edition. 59:6289-6289
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 102:135-139
The Delft total synthesis of morphinans starts from 1-benzylisoquinolines (Scheme 2, 7) and gives both the morphinans with the natural (-)-morphine configuration and the corresponding enantiomers. This route has been used as a basis for an improved s
Publikováno v:
Synlett. 2007:2863-2867
Enzymatic dihydroxylation of b-bromoethylbenzene provided a homochiral diene diol that served as starting material for the synthesis of the complete morphinan skeleton via an intramolec- ular Heck cyclization.
Autor:
Demosthenes Fokas, Kathlyn A. Parker
Publikováno v:
The Journal of Organic Chemistry. 71:449-455
[reaction: see text] The radical cyclization approach to the morphine alkaloids has been applied in an asymmetric synthesis of (-)-dihydrocodeinone. A chiral cyclohexenol (R-32), from the CBS reduction of the enone, is the source of chirality. The fi
Publikováno v:
The Journal of Organic Chemistry. 70:6492-6495
Improved protocols for the preparation of 1-bromodihydrocodeinone (1-bromohydrocodone) and 1-bromo-14-hydroxydihydrocodeinone (1-bromooxycodone) and synthesis of the corresponding 1-chloro and 1-iodo derivatives have been achieved using the correspon
Autor:
Mellar P. Davis, Jade Homsi, Susan B. LeGrand, Declan Walsh, Nabeel Sarhill, Lisa Rybicki, Kristine A. Nelson
Publikováno v:
American Journal of Hospice and Palliative Medicine®. 19:49-56
Purpose: Cough is a common symptom in advanced cancer. The use of hydrocodone as an antitussive has not been studied previously in this setting. This study evaluates hydrocodone for cough in advanced cancer. Methods: The results presented are from a
Publikováno v:
Pure and Applied Chemistry. 70:1487-1493
The concept of molecular workbenches1 is introduced and outlined in Figure 1. According to the distinction between disconnectible and non-disconnectible workbenches this account falls into two sections, the first one describing the application of aux