Asymmetric synthesis is one of the most important areas of research and development in synthetic organic chemistry, and has wide-ranging industrial applications. This introduction to the subject covers chirality, nomenclature and analytical methods of resolution. The main body of the text describes the principal methods available to the organic chemist wishing to synthesize chiral compounds. Case studies are included, and reference sections allow access to the relevant review and research literature. This book is written for organic chemists at postgraduate and advanced undergraduate level.
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Inside This Book
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First Sentence:
Asymmetric synthesis involves the formation of chiral molecules. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
original stereogenic centre, stereogenic units, chiral eluant, occurring chiral compounds, tetrahedral centre, sulphoxide group, new stereogenic centres, chemical shift nonequivalence, relative topicity, asymmetric synthesis, diastereofacial selection, substrate enantiomers, achiral substrate, chiral auxiliary, enantiomeric purity, chiral starting materials, diastereofacial selectivity, enantiomeric enrichment, enantiomerically pure compound, opposite enantiomer, lanthanide shift reagents, asymmetric reactions, enantiomeric composition, major diastereomer, solvating agents Key Phrases - Capitalized Phrases (CAPs): (learn more)
Academic Press, Tetrahedron Lett, Aldrichimica Acta, Pergamon Press New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Asymmetric synthesis involves the formation of chiral molecules. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
original stereogenic centre, stereogenic units, chiral eluant, occurring chiral compounds, tetrahedral centre, sulphoxide group, new stereogenic centres, chemical shift nonequivalence, relative topicity, asymmetric synthesis, diastereofacial selection, substrate enantiomers, achiral substrate, chiral auxiliary, enantiomeric purity, chiral starting materials, diastereofacial selectivity, enantiomeric enrichment, enantiomerically pure compound, opposite enantiomer, lanthanide shift reagents, asymmetric reactions, enantiomeric composition, major diastereomer, solvating agents Key Phrases - Capitalized Phrases (CAPs): (learn more)
Academic Press, Tetrahedron Lett, Aldrichimica Acta, Pergamon Press New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
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- Organic Chemistry, 6th Edition by Robert T. Morrison on page 62, and page 191
- Asymmetric Synthesis by H. B. Kagan on page 82, and page 190
- Chemistry and Organic Chemistry by Christopher Foote on page 191
- Organic Chemistry by Wiley on page 82
- Organic Chemistry (with Organic ChemistryNOW) by William H. Brown on page 191
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- Chiral Pollutants: Distribution, Toxicity and Analysis by Chromatography and Capillary Electrophoresis by Imran Ali on page 31, page 68, and page 144
- Principles and Applications of Stereochemistry by Michael North on page 121, and page 242
- Chirality in Industry II: Developments in the Commercial Manufacture and Applications of Optically Active Compounds by A. N. Collins in Front Matter
- Stereochemistry (Tutorial Chemistry Texts S.) by Morris on page 159
- Principles of Asymmetric Synthesis, Volume 14 (Tetrahedron Organic Chemistry) by R.E. Gawley on page 160
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