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Topics in Stereochemistry, Volume 22


Topics in Stereochemistry, Volume 22


Topics in Stereochemistry (Discontinued), Band 22 1. Aufl.

von: Scott E. Denmark

213,99 €

Verlag: Wiley
Format: PDF
Veröffentl.: 17.09.2009
ISBN/EAN: 9780470147535
Sprache: englisch
Anzahl Seiten: 336

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Beschreibungen

Since it was first published in 1967, the highly regarded Topics in Stereochemistry series has consistently reflected the state of the art in the field and provided readers with a coherent framework for the conceptual, theoretical, and practical aspects of modern stereochemistry.<br /> <br /> With the new series editor, Scott E. Denmark, at the helm, Volume 22 continues to offer important insights into the evolution of stereochemistry and its future direction. Written by internationally recognized leaders in their respective fields, this volume introduces readers to some of the most intensely studied topics in research laboratories today.<br /> <br /> Along with the fundamental principles of chirality, the authors describe exciting new applications of stereochemistry in synthetic organic, physical organic, and bioorganic chemistry. They cover cutting-edge research in areas such as asymmetric catalysis, reactions with catalytic antibodies, and stereoelectronic control of organic reactions. In addition, a feature chapter provides a critical analysis of the concepts of molecular chirality.<br /> <br /> Timely and authoritative, Topics in Stereochemistry, Volume 22, features over 120 illustrations and a cumulative index covering Volumes 1 through 22. It is an essential resource for organic chemists involved in synthesis as well as those in the physical and bioorganic areas of organic chemistry.<br /> <br /> Volume 22 relaunches this highly respected series, providing a timely, valuable reference to the theory and practice of stereochemistry. Cutting-edge topics include:<br /> * Foundations of molecular and topological chirality.<br /> * Stereoselective reactions with catalytic antibodies.<br /> * Stereoelectronic effects of the group 4 metal substituents in organic chemistry.<br /> * Asymmetric catalysis with the new class of chiral lanthanoid complexes.<br /> * Basic principles of the exciting new area of asymmetric amplification.
Molecular Chirality (K. Mislow).<br /> <br /> Stereoselective Reactions with Catalytic Antibodies (D. Hilvert).<br /> <br /> Stereoelectronic Effects of the Group 4 Metal Substituents in Organic Chemistry (J. White & C. Clark).<br /> <br /> Asymmetric Catalysis with Chiral Lanthanoid Complexes (M. Shibasaki & H. Sasai).<br /> <br /> Asymmetric Amplification (D. Fenwick & H. Kagan).<br /> <br /> Indexes.
From the review of the series: "...This excellent series is highly recommended to all chemists and is a requisite for all chemistry libraries. (<i>Journal of Medicinal Chemistry</i>) <p>"It is...welcome that, with the latest two volumes reviews here, we see a relaunch of the series.... It is beyond question that these two further volumes, like the others, should be in every library." (<i>Angewandte Chemie International Edition</i>, Vol. 42, No 13, April 4, 2003)</p> <p>"..the first volume in the relaunch of this extraordinarily useful but temporarily dormant series...Denmark has stepped forward to take on editorial duties, and he has done a splendid job...this volume belongs in the library of every college and university where organic chemistry is taught...a personal copy should be on the shelf of every scientist who is working in one or more of the areas covered and in the personal library of any professor who teaches advanced level courses..." (<i>Journal of the American Chemical Society</i>, Vol. 125, No. 28)</p>
<p><b>SCOTT E. DENMARK</b> is the R. C. Fuson Professor of Chemistry at the University of Illinois at Urbana-Champaign. In addition to his editor-in-chief role for <i>Organic Reactions</i>, he is an editor for <i>Organic Syntheses</i> and for the <i>Encyclopedia of Reagents for Organic Synthesis</i>, both available from Wiley.</p>
Since it was first published in 1967, the highly regarded Topics in Stereochemistry series has consistently reflected the state of the art in the field and provided readers with a coherent framework for the conceptual, theoretical, and practical aspects of modern stereochemistry. <p>With the new series editor, Scott E. Denmark, at the helm, Volume 22 continues to offer important insights into the evolution of stereochemistry and its future directions. Written by internationally recognized leaders in their respective fields, this volume introduces readers to some of the most intensely studied topics in research laboratories today.</p> <p>Along with the fundamental principles of chirality, the authors describe exciting new applications of stereochemistry in synthetic organic, physical organic, and bioorganic chemistry. They cover cutting-edge research in areas such as asymmetric catalysis, reactions with catalytic antibodies, and stereoelectronic control of organic reactions. In addition, a feature chapter provides a critical analysis of the concepts of molecular chirality.</p> <p>Timely and authoritative, Topics in Stereochemistry, Volume 22, features over 120 illustrations and a cumulative index covering Volumes 1 through 22. It is an essential resource for organic chemists involved in synthesis as well as those in the physical and bioorganic areas of organic chemistry.</p> <p>"This excellent series is highly recommended to all chemists and is a requisite for all chemistry libraries."—Journal of Medicinal Chemistry</p> <p>Volume 22 of Topics in Stereochemistry relaunches this highly respected series, providing a timely, valuable reference to the theory and practice of stereochemistry. Cutting-edge topics include:</p> <ul> <li>Foundations of molecular and topological chirality</li> <li>Stereoselective reactions with catalytic antibodies</li> <li>Stereoelectronic effects of the group 4 metal substituents in organic chemistry</li> <li>Asymmetric catalysis with the new class of chiral lanthanoid complexes</li> <li>Basic principles of the exciting new area of asymmetric amplification</li> </ul>

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