Titlebook: New Developments in Molecular Chirality; Paul G. Mezey Book 1991 Springer Science+Business Media Dordrecht 1991 Dichroism.Vibration.ab ini

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A global approach to molecular chirality,ble arrangements of a given stoichiometric family of nuclei are considered. Such a stoichiometric family includes all isomers, intermediates and decomposition products of all molecules and their transition structures with a given atomic composition, as well as all distorted conformations of the abov

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Book 1991lecules of exceptional structural properties. Some of the new developments in molecular chirality have been truly fundamental to the theoretical understanding and to the actual practice of many aspects of chemistry. The progress in this field has been very rapid, even accelerating in recent years, a

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to new molecules of exceptional structural properties. Some of the new developments in molecular chirality have been truly fundamental to the theoretical understanding and to the actual practice of many aspects of chemistry. The progress in this field has been very rapid, even accelerating in recent years, a978-94-010-5644-1978-94-011-3698-3

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Vibrational Circular Dichroism Intensities: , Calculations, stereochemical information. Since the earliest theoretical models [.] and the first successful experimental measurements [.,.], VCD has seen rapid advances in instrumentation and theory. Reliable measurements over most of the vibrational spectrum can be carried out, and reliable theoretical computa

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Chiral Features of Proteins,pability to determine their three-dimensional structures by x-ray crystallographic, and lately by 2D-NMR methods, has led to a flurry of activity in the development and application of new methods to analyze their structural features [.,.]. A striking feature of proteins, and in fact of all biomacrom

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A Topological Hierarchy of Molecular Chirality and other Tidbits in Topological Stereochemistry,ph was first invented to explain isomerism, including the classifications used in modern stereochemistry. Thus, constitutional isomers describe pairs of isomeric molecular structures possessing non-homeomorphic molecular graphs, while the classical stereoisomers (enantiomers and diastereomers) posse

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