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Titlebook: Basic Concepts in Organic Stereochemistry; Sunil Kumar Talapatra,Bani Talapatra Book 2022 The Editor(s) (if applicable) and The Author(s),

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發(fā)表于 2025-3-21 19:05:09 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Basic Concepts in Organic Stereochemistry
影響因子2023Sunil Kumar Talapatra,Bani Talapatra
視頻videohttp://file.papertrans.cn/181/180983/180983.mp4
發(fā)行地址Presents essential stereochemical concepts of organic molecules.Illustrative examples to aid discussion.Easy-to-read overview of natural products
圖書封面Titlebook: Basic Concepts in Organic Stereochemistry; Sunil Kumar Talapatra,Bani Talapatra Book 2022 The Editor(s) (if applicable) and The Author(s),
影響因子This book discusses essential stereochemical concepts associated with organic molecules (natural or synthetic), as reflected in the course of their many reactions, their mechanisms, their asymmetric synthesis, biosynthesis, and biological activities. This treatise provides useful insights and understanding of the chiral/achiral designations (nomenclatures), the stereochemical features, and related properties of the natural and synthetic products. Without having an adequate knowledge of stereochemical concepts, it will not be possible to understand and appreciate the stereochemistry of natural or synthetic products. Thus, essential static and dynamic aspects of stereochemistry with sufficient illustrative examples along with discussions are presented. The structure of the monograph allows for easy selection of separate topics for reading and teaching. This book will also provide an idea of basic stereochemical concepts, as applied to organic molecules in general as well as to organic ligands in coordination complexes, and will, therefore, be valuable resources to teachers and students of advanced undergraduates and post-graduates, researchers, and professionals..
Pindex Book 2022
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Chiroptical Properties I: Optical Rotation. ORD, CD,s applications with examples; absolute configuration of .-decalones through octant rule; CE signs (observed—same as predicted) of octant projection diagrams (opds) of a few perhydrophenanthrenones and perhydroanthracenones, some cholestanones and coprostanones.
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https://doi.org/10.1007/978-3-662-57974-9s applications with examples; absolute configuration of .-decalones through octant rule; CE signs (observed—same as predicted) of octant projection diagrams (opds) of a few perhydrophenanthrenones and perhydroanthracenones, some cholestanones and coprostanones.
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https://doi.org/10.1007/978-3-658-25600-5acids, cis- and trans-1,2-dihaloethylenes; solubilities (in water) of maleic and fumric acids, cis- and trans-crotonic acids, cis- and trans-cinnamic acids; boiling points, densities, refractive indices of geometrical isomers; and acid strengths of monobasic acids: cis- and trans-crotonic acids, dibasic acids: maleic acid and fumaric acid.
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Configurational Nomenclature. Physical Properties of Geometrical Isomers,acids, cis- and trans-1,2-dihaloethylenes; solubilities (in water) of maleic and fumric acids, cis- and trans-crotonic acids, cis- and trans-cinnamic acids; boiling points, densities, refractive indices of geometrical isomers; and acid strengths of monobasic acids: cis- and trans-crotonic acids, dibasic acids: maleic acid and fumaric acid.
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Cyclohexanone,rotonation by Avoiding Allylic. Strain; Conformation of Cyclohexene, Allylic. Strain, Conformational Preference of Substituted Cyclohexenes, Synthesis of Solenopsin A—Application of A. Strain Concept; and Pseudoallylic 1,2 Strain in Enamines.
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