Stereochemistry of Organic Compounds: Principles and ApplicationsDuring Recent Years, Stereochemistry Has Undergone A Phenomenal Growth Both In Theory And Practice, With A Concomitant Increase Of Interest Among The Organic Chemists, Biological Chemists, Medicinal Chemists, And Pharmacologists. The Present Text Provides An Up-To-Date, Coherent; And Comprehensive Account Of The Subject Starting From The Fundamentals And Leading Up To The Latest Development As Far As Practicable. Emphasis Has Been Placed On Symmetry-Based Approach To Molecular Chirality, Stereochemical Terminologies (Modern Stereochemistry Is Replete, With Them), Topicity And Prostereoisomerism, Conformational Analysis, Dynamic Stereochemistry, Chiroptical Properties, And Assignment Of Absolute Configuration To Chiral Molecules.Dynamic Stereochemistry Has Been Discussed With Reference To Conformation-Reactivity Correlation, Stereoselective Syntheses, And Pericyclic Reactions. A Large Cross Section Of Organic Reactions With Stereochemical Implication Has Been Incorporated. Attempts Have Been Made To Familiarise The Readers With Modem Instrumental Techniques, Nuclear Magnetic Resonance In Particular, Used For Stereochemical Investigation. Each Chapter Is Provided With A Summary Which Highlights The Main Points Of The Text. Selective References, Mostly Of Textbooks, Monographs, Review Articles, And Significant Original Papers Have Been Given Extending Sometimes To Early 1991.The Book Is Expected To Fulfil The Long-Felt Need For A Comprehensive Text On Modern Organic Stereochemistry Which Is Conspicuously Absent Since The Publication Of Professor Eliels Book In 1962. The Text May Be Adopted At Any Stage Of The University Teaching And At The Same Time Be Useful To The Practising Organic Chemists. |
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I love this book. But sadly there is no way to download or watch yhis complete book.
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All 10 reviews »love this book...but please make the way so that we can downlad the book....as its really important due to lockdown as shops are closed
Contents
Molecular Geometry and Chemical Bonding | 1 |
Molecular Symmetry and Chirality | 15 |
Definitions and Classifications | 27 |
Stereoisomerism and Centre of Chirality | 43 |
Axial Chirality Planar Chirality | 72 |
Topicity and Prostereoisomerism | 106 |
Racemisation and Methods of Resolution | 135 |
Determination of Configuration | 163 |
Chapter 10 | 240 |
Fused Ring | 306 |
Conformation and Reactivity | 339 |
Stereoselective Reactions | 404 |
Chapte | 478 |
Chemical Stereochemical | 509 |
545 | |
Conformations of Acyclic Molecules | 203 |
Common terms and phrases
achiral acid addition alcohols Amer angle anti asymmetric atoms axial axis barrier bond called carbon chair Chapter Chem chemical chiral centre CO2H complex components compounds configuration conformers containing corresponding cyclic cyclic compounds cyclohexane depends derivatives determined diastereomers direction discussed double bond effect electrons Eliel enantiomeric enantiomers energy equatorial erythro example exists faces Figure formation four gauche given gives glucose hand higher hydrogen increases interaction inversion isomer ketones kJ mol known leads ligands lone pair method molecular molecules nature orbital Organic pair plane point group position preferred presence principle properties provides racemic reaction reagents rearrangement reduction relative respectively result ring rotation rule shift shown side similar single specific stable stereochemistry stereoisomers stereoselectivity steric strain structure substituents substrate symmetry synthesis temperature torsion trans transition usually values York