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Conformational Concept For Synthetic Chemist's Use: Principles and in Lab Exploitation, by Anatoly M Belostotskii
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This innovative book presents an original account of the principles of conformational theory. It has a strong focus on computational methodologies for conformational space exploration. By revisiting basic conformational conventions, considering experimental results which are often misinterpreted by organic chemists, and qualitatively analyzing the potential energy surface, the book helps non-experts to understand molecular flexibility at the level required in contemporary research.
The book shows synthetic organic chemists how to perform successful conformational studies using widespread calculation packages ('click computational chemistry') instead of being misguided by textbook-based conformational analysis. The monograph actually offers to synthetic chemists a new research tool that can significantly upgrade their ability to predict, or at least explain, regioselectivity and stereoselectivity in their own reactions.
Readership: Organic, bioorganic, and medicinal chemists, specialists in structure determination of natural products, drug and material designers; advanced graduate students.
- Sales Rank: #5551504 in Books
- Published on: 2015-11-18
- Original language: English
- Number of items: 1
- Dimensions: 9.25" h x 6.25" w x 1.50" l, .0 pounds
- Binding: Hardcover
- 580 pages
About the Author
Anatoly M. Belostotskii, KAMEA Associate Professor, Bar-Ilan University [Ph.D. on synthetic stereochemical studies, in the Academician Ivan L. Knunyantz's ("Knunyantz The Great") laboratory, Moscow; postdoctoral studies on conformational dynamics, in the Professor Alfred Hassner's group; current research includes cancer-targeting nucleoside chemistry as well as development of computational conformational analysis]: "Organic chemistry, biochemistry and medicinal chemistry have been re-shaped after accepting conformational ideas in the 60s. Regrettably, a majority of organic experimentalists at all academic levels ubiquitously use general conformational models of that times and do not assume that this analysis actually is speculative. You can guess the ineluctable result of this practice — unbased conclusions and misinterpretations are scattered in chemical literature. The good news is that computational conformational analysis is a simple way to benefit from the genuine fruitfulness of conformational theory. I think that an advanced organic experimentalist certainly should be capable of freely operating with basic computational chemistry; nowadays, this is easy."
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