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Author Gawley, Robert E.

Title Principles of asymmetric synthesis / Robert E. Gawley and Jeffrey Aubé.

Imprint Oxford, U.K. ; Tarrytown, N.Y. : Pergamon, ©1996.

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Location Call No. OPAC Message Status
 Axe Elsevier ScienceDirect Ebook  Electronic Book    ---  Available
Edition 1st ed.
Description 1 online resource (xvii, 372 pages) : illustrations
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
Series Tetrahedron organic chemistry series ; v. 14
Tetrahedron organic chemistry series ; v. 14.
Bibliography Includes bibliographical references and index.
Contents Introduction -- Analytical methods -- Enolate, azaenolate, organolithium alkylations -- 1,2 and 1,4 additions to carbonyls -- Aldol and Michael additions of allyls and enolates -- Rearrangements and cycloadditions -- Reductions and hydoborations -- Oxidations -- Index.
Note Print version record.
Summary The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed
Language English.
Subject Asymmetric synthesis.
Synthèse asymétrique.
SCIENCE -- Chemistry -- Organic.
Asymmetric synthesis
Synthese (chemie)
Chiraliteit.
Enantiomeren.
Synthèse asymétrique.
Composés organiques.
Added Author Aubé, Jeffrey.
Other Form: Print version: Gawley, Robert E. Principles of asymmetric synthesis. 1st ed. Oxford, U.K. ; Tarrytown, N.Y. : Pergamon, ©1996 0080418767 9780080418766 (DLC) 97122813 (OCoLC)36166000
ISBN 9780080514772 (electronic bk.)
0080514774 (electronic bk.)
9780080418759
0080418759
9786611981785
6611981780
1281981788
9781281981783
0080418767 (Hardcover)
0080418759 (Flexicover)
9780080418766
Standard No. AU@ 000051558529
CHDSB 005988980
DEBBG BV039828639
DEBBG BV042313865
DEBBG BV043091353
DEBSZ 367768771
DEBSZ 422019879
DEBSZ 482359013
GBVCP 588451452
GBVCP 802808913
NZ1 12433177
NZ1 15188857

 
    
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