Synthese neuartiger Inhibitoren der humanen delta8,7-Sterolisomerase - Taschenbuch
ISBN: 3868538666
Taschenbuch, [EAN: 9783868538663], Dr. Hut, Dr. Hut, Book, Dr. Hut, Dr. Hut, 290522, Medizin, 404348, Allgemeinmedizin, 404350, Alternative Heilmethoden, 295134, Anästhesie, 296942, Chiru… Mehr…
amazon.de verlag_dr_hut [Rating: 4.8] Neuware Versandkosten:Innerhalb EU, Schweiz und Liechtenstein (soferne Lieferung möglich) (EUR 3.00) Details... |
Synthese neuartiger Inhibitoren der humanen delta8,7-Sterolisomerase - Taschenbuch
ISBN: 3868538666
Taschenbuch, [EAN: 9783868538663], Dr. Hut, Dr. Hut, Book, Dr. Hut, Dr. Hut, 290522, Medizin, 404348, Allgemeinmedizin, 404350, Alternative Heilmethoden, 295134, Anästhesie, 296942, Chiru… Mehr…
Bibliographische Daten des bestpassenden Buches
Autor: | |
Titel: | |
ISBN-Nummer: |
Detailangaben zum Buch - Synthese neuartiger Inhibitoren der humanen delta8,7-Sterolisomerase
ISBN (ISBN-10): 3868538666 (ISBN-13: 9783868538663)
Taschenbuch
Buch in der Datenbank seit 2011-08-11T11:12:02+02:00 (Berlin)
Detailseite zuletzt geändert am 2011-08-11T11:12:02+02:00 (Berlin)
ISBN/EAN: 3868538666
ISBN - alternative Schreibweisen:
3-86853-866-6
Alternative Schreibweisen und verwandte Suchbegriffe:
Titel des Buches: delta
Daten vom Verlag:
Autor/in: Mathias König
Titel: Pharmazeutische Chemie; Synthese neuartiger Inhibitoren der humanen delta8,7-Sterolisomerase
Verlag: Dr. Hut
Erscheinungsjahr: 2011-04-15
Gewicht: 0,446 kg
51,00 € (DE)
52,50 € (AT)
Not available (reason unspecified)
BC; PB; Hardcover, Softcover / Medizin/Pharmazie; Pharmazie, Apotheke; Medizin, Gesundheit
Homogeneous catalysts based on transition metals are of high industrial relevance. An important goal for this purpose is the light-induced start of the catalytic reaction. The electronic and steric influence of the olefin ligand upon the spectroscopic properties, stability and reactivity of bistriphenylphosphine-cinnamate and related complexes of group 10 were studied in this thesis. By means of these findings a direct prediction of the reactivity was possible based on the NMR-spectroscopic behaviour. Thus a specific design of photo-switchable complexes was possible, in which the olefin ligand could be cleaved from the metal via a selective light-induced intra-ligand cyclisation. This ring closure was examined with the ligand itself as well as in the complexes, concerning electronic and steric influences.< zum Archiv...