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005 | 20170713221426.0 | ||
006 | m o d | ||
007 | cr cnu---unuuu | ||
008 | 151002s2015 gw ob 001 0 eng d | ||
040 |
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019 | _a959250327 | ||
020 |
_a9783527684199 _qelectronic bk. |
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020 |
_a3527684190 _qelectronic bk. |
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020 |
_a9783527684205 _qelectronic bk. |
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020 |
_a3527684204 _qelectronic bk. |
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020 | _z9783527337491 | ||
029 | 1 |
_aDEBBG _bBV043738064 |
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035 |
_a(OCoLC)922698100 _z(OCoLC)959250327 |
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050 | 4 | _aQC174.17.S9 | |
072 | 7 |
_aSCI _x057000 _2bisacsh |
|
082 | 0 | 4 |
_a539.725 _223 |
049 | _aMAIN | ||
100 | 1 |
_aGlaser, Robert, _eauthor. |
|
245 | 0 | 0 |
_aSymmetry, spectroscopy, and crystallography : _bthe structural nexus / _cRobert Glaser. |
264 | 1 |
_aWeinheim : _bWiley-VCH, _c2015. |
|
300 | _a1 online resource. | ||
336 |
_atext _btxt _2rdacontent |
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337 |
_acomputer _bc _2rdamedia |
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338 |
_aonline resource _bcr _2rdacarrier |
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505 | 0 | _aSymmetry/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 Structure -- Historical Development of Structural Chemistry: From Alchemy to Modern Structural Theory -- Chiroptical Properties -- Symmetry Comparison of Molecular Subunits: Symmetry in Nuclear Magnetic Resonance Spectroscopy and 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. | |
504 | _aIncludes bibliographical references and index. | ||
588 | 0 | _aOnline resource; title from PDF title page (EBSCO, viewed October 7, 2015) | |
650 | 0 | _aSymmetry (Physics) | |
650 | 0 | _aCrystallography. | |
650 | 0 | _aStereochemistry. | |
650 | 7 |
_aSCIENCE / Physics / Quantum Theory _2bisacsh |
|
650 | 7 |
_aCrystallography. _2fast _0(OCoLC)fst00884652 |
|
650 | 7 |
_aStereochemistry. _2fast _0(OCoLC)fst01133138 |
|
650 | 7 |
_aSymmetry (Physics) _2fast _0(OCoLC)fst01140819 |
|
655 | 4 | _aElectronic books. | |
856 | 4 | 0 |
_uhttp://onlinelibrary.wiley.com/book/10.1002/9783527684199 _zWiley Online Library [Free Download only for SUST IP] |
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_aIngram Digital eBook Collection _bIDEB _ncis31546462 |
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_aRecorded Books, LLC _bRECE _nrbeEB00627701 |
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