|The Nuclear Overhauser Effect in Structural and Conformational Analysis, 2nd Edition
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Author: David Neuhaus
An authoritative review of the state of the art in the Nuclear Overhauser Effect-essential information for organic chemists, biochemists, biophysicists, and NMR spectroscopists
The field of NMR spectroscopy has seen tremendous growth in the last twenty years, particularly advances relating to Nuclear Overhauser Effect (NOE) spectroscopy-the most powerful technique for obtaining structural information on molecules in solution. Extensive and engaging, the Second Edition of the leading reference on the NOE is significantly updated to reflect the latest changes and new approaches in the field.
Neuhaus and Williamson provide an essential guide to the complexities and use of the NOE in a readily accessible, straightforward manner. Their practical handbook features a new chapter addressing the use of NOE data to calculate biomolecular structures. Chapters dealing with the kinetics of the NOE, the effects of exchange and internal motion, and applications of the NOE, are also extensively revised. Cross-referenced in remarkable depth, The Nuclear Overhauser Effect is organized into three main parts:
* Part I describes the theory of the Nuclear Overhauser Effect in a clear, comprehensive fashion
* Part II discusses the considerations involved in implementing NOE experiments, including full coverage of all necessary details for both new and established techniques
* Part III offers examples of how the NOE is used, including applications to defining molecular geometry, stereochemistry, conformation, and biomolecular structure and interactions
The Nuclear Overhauser Effect in Structural and Conformational Analysis, Second Edition, uniquely explains the NOE in detail, making it an indispensable resource for the novice as well as the experienced NMR researcher.
|Stereoelectronic Effects in Organic Chemistry
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Author: Pierre Deslongchamps
Stereoelectronic effects in organic chemistry.
|Reflections on Symmetry in Chemistry and Elsewhere
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Author: Edgar Heilbronner
Brand: Brand: VCH Publishers
What do Schrödinger's wave functions, Escher's intricate tiling patterns and chemistry's latest marvel, buckminsterfullerene, have in common?
This stunning book, written by two world-famous scientists, introduces the reader to one of nature's most fundamental, and ubiquitous, phenomena: Symmetry.
Enormous in scope, this scientific tour-de-force covers topics as diverse as quantum mechanics, stereochemistry, Penrose tilings and Raphael's Madonna. The authors connect these apparently unrelated fields in a completely non-mathematical fashion, which should appeal to the general and specialist reader alike.
Lucidly written and beautifully illustrated, this book provides an eminently readable discussion of the omnipresent concept of symmetry, its application in all branches of science, and its perception in nature, art and elsewhere.
- Used Book in Good Condition
|Stereochemistry and Stereoselective Synthesis: An Introduction
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Author: MihÃ¡ly NÃ³grÃ¡di
Written by a well-respected and experienced author, this textbook fills the gap for a concise introduction to the key concepts of organic stereochemistry and the most important classical and modern methods in stereoselective synthesis.
The concepts are extensively illustrated in color, with practical examples and question-answer sets to help consolidate the reader's knowledge. In addition, animations are available from the Wiley website.
A must-have for students in chemistry, biochemistry, and life sciences, as well as researchers in pharmaceutical and agrochemical companies in need of a quick introduction to the field.
|Introduction to Stereochemistry
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Author: Kurt Mislow
Three-part introductory text reviews molecular architecture, relating empirical bonding geometries to hybridization of central carbon atom; classifies stereoisomers according to symmetry properties and to nature of their barriers; and explores conceptual basis of asymmetric syntheses and kinetic resolutions. Exercises with answers. 1965 edition.
|Asymmetric Synthesis: The Chiral Carbon Pool and Chiral Sulfur, Nitrogen, Phosphorus, and Silicon Centers
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Author: James D. Morrison
|Carbon-Carbon and Carbon-Proton Nmr Couplings: Applications to Organic Stereochemistry and Conformational Analysis (Methods in Stereochemical Analysis)
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Author: James L. Marshall
Brand: Brand: Vch Pub
This comprehensive survey of long-range carbon-proton (13C-1H) and carbon-carbon (13C-13C) couplings contains all the information needed to apply successfully this advanced method of instrumental analysis. It discusses the special considerations that apply particularly to the acquisition of carbon coupling data via Fourier transform NMR spectroscopy and refers to corresponding proton-proton couplings in cases where they apply to carbon-proton and carbon-carbon couplings. It also gives particular attention to the troublesome problem of determining the signs of carbon couplings.
- Used Book in Good Condition
|Neurostereology: Unbiased Stereology Of Neural Systems
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Author: Peter R. Mouton
Stereological methods provide researchers with unparalleled quantitative data from tissue samples and allow for well-evidenced research advances in a broad range of scientific fields. Presenting a concise introduction to the methodology and application of stereological research in neuroscience, Neurostereology provides a fuller understanding of the use of these methods in research and a means for replicating successful scientific approaches. Providing sound footing for future research, Neurostereology is a useful tool for basic and clinical researchers and advanced students looking to integrate these methods into their research.
|Electromagnetic Waves in Chiral and Bi-Isotropic Media (Artech House Antenna Library)
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Author: A.H. Sihvola
Brand: Ismo V Lindell
For scientists, research engineers, physicists and postgraduate students, this work introduces the essential aspects of electromagnetic waves in chiral and bi-isotropic media, to give the practical working knowledge necessary for new application development. It includes sections on effective methods of measurement, how chiral and BI media affect electromagnetic fields and wave propagation, and how to apply the theory to basic problems in waveguide, antenna and scattering analysis.
- Electromagnetic Waves In Chiral And Bi Isotropic Media
|CRC Handbook of Optical Resolutions via Diastereomeric Salt Formation
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Optically active compounds are gaining ever-increasing importance in organic chemistry, both in the academic and the industrial arenas. The rational synthesis of the growing number of chiral chemicals, drugs, and natural products demands efficient methods for producing these compounds in an enantiomerically, highly pure form. Despite the available alternative techniques, optical resolution via Diastereomeric salt formation remains the most widely used method of preparing pure enantiomers.
The CRC Handbook of Optical Resolutions Via Diastereomeric Salt Formation is the first book to exclusively address this important organic chemical process. It provides fast, one-stop access to a wealth of information, including all of the available data on 100 resolving agents, a list of 500 optically active compounds available in bulk along with their suppliers, data on more than 3,500 resolutions, and 4,200 citations.
This handbook helps answer virtually any question that may arise during the development of a new resolution process.
Which resolving agent and solvent should I use under these conditions?
How can I separate the diastereoisomers?
How can I optimize a resolution process?
How do I determine enantiomeric purity?
Which supplier has the resolving agent I need?
For a racemate already resolved, what were the resolving agent, solvent, and relevant citation?
This is the first book to deal exclusively with all aspects of this important organic chemical process, both theoretical and practical. With an abundance of analyzed examples, this single, authoritative reference provides all of the information you need to perform, develop, and optimize optical resolutions via Diastereomeric salt formation