Showing posts with label oxford. Show all posts
Showing posts with label oxford. Show all posts

Friday, September 16, 2011

The Role of Chromosomal Change in Plant Evolution (Oxford Series in Ecology and Evolution)

The Role of Chromosomal Change in Plant Evolution (Oxford Series in Ecology and Evolution) Review


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The Role of Chromosomal Change in Plant Evolution (Oxford Series in Ecology and Evolution) Feature

The application of molecular technology has greatly increased our understanding of the role of chromosomal change in plant evolution. There is now a broad database on genome size variation within and among species and a wide array of nuclear and cytoplasmic genetic markers. There is a variety of literatures addressing this subject but much of it is scattered. This book created a contemporary synthesis of work in this area and addresses issues such as heterogeneity, polyploidy, chromosomal rearrangements within species and phenotypic consequences of chromosome doubling.


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Sunday, June 12, 2011

Organic Stereochemistry (Oxford Chemistry Primers)

Organic Stereochemistry (Oxford Chemistry Primers) Review


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Organic Stereochemistry (Oxford Chemistry Primers) Feature

Number 88 in the well-known Oxford Chemistry Primer series introduces upper-undergraduate students to how the three-dimensional shapes of molecules influence their chemical and physical properties. It starts with an introduction to common stereochemical terms used throughout the book. Chapter two covers 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. 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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