Organic Stereochemistry (Oxford Chemistry Primers)

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9780198792758: Organic Stereochemistry (Oxford Chemistry Primers)
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Book by Robinson Michael J T

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Críticas:

"Provides an account of how the three dimensional shapes of molecules influence their chemical and physical properties. Begins with material on the structures of molecules, then describes how such structures can be changed. A description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relative configurations of molecules and topism. Racemates, their resolutions, and methods for determining enantiomeric purity are discussed. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries. Includes problems with hints and answers. Robinson teaches organic chemistry at Magdalen College, University of Oxford."--SciTech Book News "Provides an account of how the three dimensional shapes of molecules influence their chemical and physical properties. Begins with material on the structures of molecules, then describes how such structures can be changed. A description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relative configurations of molecules and topism. Racemates, their resolutions, and methods for determining enantiomeric purity are discussed. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries. Includes problems with hints and answers. Robinson teaches organic chemistry at Magdalen College, University of Oxford."--SciTech Book News "Provides an account of how the three dimensional shapes of molecules influence their chemical and physical properties. Begins with material on the structures of molecules, then describes how such structures can be changed. A description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relative configurations of molecules and topism. Racemates, their resolutions, and methods for determining enantiomeric purity are discussed. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries. Includes problems with hints and answers. Robinson teaches organic chemistry at Magdalen College, University of Oxford."--SciTech Book News "Provides an account of how the three dimensional shapes of molecules influence their chemical and physical properties. Begins with material on the structures of molecules, then describes how such structures can be changed. A description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relative configurations of molecules and topism. Racemates, their resolutions, and methods for determining enantiomeric purity are discussed. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries. Includes problems with hints and answers. Robinson teaches organic chemistry at Magdalen College, University of Oxford."--SciTech Book News

Reseña del editor:

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 of acyclic 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 relative configurations 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 for predicting stereoselectivity, and double asymmetric synthesis.

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