Organic Stereochemistry by Michael Robinson

Organic Stereochemistry

byMichael Robinson

Paperback | March 31, 2000

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A short historical introduction serves to introduce many common stereochemical terms used throughout the book. Chapter two is an account of the structures of simple unstrained organic molecules followed by examples of strained molecules. The third chapter deals with conformational analysis ofacyclic and carbocyclic molecules, ending with a short exposition of molecular mechanics. Chapter four is about stereoisomerism in molecules and compounds. A full description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relativeconfigurations of molecules and for topism. A short chapter describes racemates, their resolution, and methods for determining enantiomeric purity. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries, rules forpredicting stereoselectivity, and double asymmetric synthesis.

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Dr Michael J T Robinson MA Dphil, Magdalen College, University of Oxford, Oxford OX1 4AU
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Title:Organic StereochemistryFormat:PaperbackPublished:March 31, 2000Publisher:Oxford University PressLanguage:English

The following ISBNs are associated with this title:

ISBN - 10:0198792751

ISBN - 13:9780198792758

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Table of Contents

IntroductionDevelopments of methods and concepts in organic stereochemistryOrganic moleculesShapes, Sizes and Strain problemsThe changing shapes of organic moleculesProblemsStereoisomerism in molecules and compoundsProblemsRacemates and resolutionStereospecific and stereoselective reactionsProblemsAnswers and hints