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Autore: | Glaser Robert |
Titolo: | Symmetry, spectroscopy, and crystallography : the structural nexus / / Robert Glaser |
Pubblicazione: | Weinheim, Germany : , : Wiley-VCH, , 2015 |
©2015 | |
Descrizione fisica: | 1 online resource (345 pages) : illustrations, tables |
Disciplina: | 548 |
Soggetto topico: | Crystallography |
Symmetry (Physics) | |
Stereochemistry | |
Cristal·lografia | |
Simetria (Física) | |
Estereoquímica | |
Soggetto genere / forma: | Llibres electrònics |
Nota di bibliografia: | Includes bibliographical references and index. |
Nota di contenuto: | Symmetry/Pseudosymmetry: Chirality in molecules, in nature, and in the cosmos -- Enantiospecificity of pheromones, sweeteners, fragrances, and grugs -- Bonding parameters and the effect of local environment on molecular -- Historical development of structural chemistry: from alchemy to modern structural theory -- Chiroptical properties -- Symmetry comparison of molecular subunits: symmetry in nuclear magnetic resonance spectroscopy ans in dynamic NMR -- Prochirality, Asymmetric hydrogenation reactions, and the curtin-Hammett principle -- Stereogenic elements, chirotopicity, permutational isomers, and gear-like correlated motion of molecular subunits -- Symmetry in extended periodic arrays of molecular tiling rules for nonperiodi quasicrystal packing -- Multiple molecules in the asymmetric unit, "faking it". pseudosymmetri emulation of achiral higher order space filling in Kryptoracemate chiral crystals -- Platonic-Solid geometry molecules and crystallographic constraints upon molecular geometry, Symmetry distortions from ideality -- Solid-State NMR Spectroscopic/X-rat crystallographic investigation of conformational polymorphism/Pseudopolymorphism in crystalline stable and labile hydrated drugs -- NMR spectroscopic diffentiation of diastereomeric isomers having special positions of moleculat symmetry -- Stereochemistry of medium ring conformations -- The pharmacophore method assisted drug design -- The X-ray structure-based method of rational design -- elical Stereochemistry. |
Symmetry/Pseudosymmetry: Chirality in molecules, in nature, and in the cosmos -- Enantiospecificity of pheromones, sweeteners, fragrances, and drugs -- Bonding parameters and the effect of local environment on molecular -- Historical development of structural chemistry: from alchemy to modern structural theory -- Chiroptical properties -- Symmetry comparison of molecular subunits: symmetry in nuclear magnetic resonance spectroscopy ans in dynamic NMR -- Prochirality, Asymmetric hydrogenation reactions, and the Curtin-Hammett principle -- Stereogenic elements, chirotopicity, permutational isomers, and gear-like correlated motion of molecular subunits -- Symmetry in extended periodic arrays of molecular crystals and the relevance of Penrose tiling rules for nonperiodic quasicrystal packing -- Multiple molecules in the asymmetric unit, "faking it". pseudosymmetry emulation of achiral higher order space filling in Kryptoracemate chiral crystals -- Platonic-Solid geometry molecules and crystallographic constraints upon molecular geometry, Symmetry distortions from ideality -- Solid-State NMR Spectroscopic/X-ray crystallographic investigation of conformational polymorphism/Pseudopolymorphism in crystalline stable and labile hydrated drugs -- NMR spectroscopic differentiation of diastereomeric isomers having special positions of molecular symmetry -- Stereochemistry of medium ring conformations -- The pharmacophore method for computer assisted drug design -- The X-ray structure-based method of rational design -- Helical Stereochemistry. | |
Titolo autorizzato: | Symmetry, spectroscopy, and crystallography |
ISBN: | 3-527-68421-2 |
3-527-68419-0 | |
3-527-68420-4 | |
Formato: | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione: | Inglese |
Record Nr.: | 9910830008103321 |
Lo trovi qui: | Univ. Federico II |
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