[PDF] Reductions By The Alumino And Borohydrides In Organic Synthesis eBook

Author : Jacqueline Seyden-Penne
Publisher : John Wiley & Sons
Page : 244 pages
File Size : 41,42 MB
Release : 1997-09-01
Category : Science
ISBN : 9780471190363

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A complete guide to selection and use of the best reagents for a wide range of transformations This book is the updated and expanded Second Edition of Jacqueline Seyden-Penne's practical guide to selection of reducing reagents in organic synthesis. It is an indispensable working resource for organic synthetic chemists-the only reference focusing exclusively on aluminohydrides and borohydrides and their derivatives. Simple to use, it is organized according to specific reductions so that chemists can more easily match the best reagent to a given transformation. Throughout, Dr. Seyden-Penne emphasizes four crucial categories: compatibility, possibilities for partial reduction, the regio- and stereoselectivity of reductions that are altered or controlled by neighboring groups, and asymmetric reductions. Extremely well-referenced, Reductions by the Alumino- and Borohydrides in Organic Synthesis provides the most up-to-date, detailed coverage of: * Successful techniques for performing highly selective reductions * Chemo-, regio-, stereo-, and enantioselective reductions of both simple and complex compounds * Best methods for obtaining the main functional groups by hydridereduction, provided in quick-reference tabular form * New and more selective reagents developed within the last five years * Experimental conditions, including solvent and temperature, and yields for most cases described.

Author : Seyden-Penne
Publisher : Vch Pub
Page : 194 pages
File Size : 19,6 MB
Release : 1991-06-01
Category : Science
ISBN : 9780471188070

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This easy-to-use guide allows the reader to select the right reagent for the desired reduction employed in organic synthesis. Topics given special emphasis in this work include: the compatibility between the reduction of the group in question and other functional groups partial reduction regio- and stereo selectivity of reductions. A foreword by Nobel Laureate H.C. Brown is also included. Three convenient sections cover: the enumeration on the most useful reagents reactivity of the functional groups towards reducing reagents access by hydride reduction of the main functions groups of organic chemistry in the form of synoptic tables.

Author : Ahmed F. Abdel-Magid
Publisher :
Page : 248 pages
File Size : 11,41 MB
Release : 1996
Category : Science
ISBN :

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Describes recent advances in reduction, including the use of boron- and aluminum-based hydride reagents, as well as catalytic hydrogenation methods. Reports applications of reduction procedures with emphasis on selectivity, ranging from chemoselective to enantioselective reductions. Offers chapters on different aspects of reduction and presents a complementary mix of academic and industrial research ranging from theory to practical applications. Includes an overview chapter with 200 references by Nobel laureate H.C. Brown that surveys the development of hydride reduction in organic chemistry over the past 60 years.

Author : Reinhard Bruckner
Publisher : Elsevier
Page : 636 pages
File Size : 50,62 MB
Release : 2001-08-03
Category : Science
ISBN : 0080498809

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A best-selling mechanistic organic chemistry text in Germany, this text's translation into English fills a long-existing need for a modern, thorough and accessible treatment of reaction mechanisms for students of organic chemistry at the advanced undergraduate and graduate level. Knowledge of reaction mechanisms is essential to all applied areas of organic chemistry; this text fulfills that need by presenting the right material at the right level.

Author : Jie Jack Li
Publisher : Oxford University Press
Page : 219 pages
File Size : 39,80 MB
Release : 2007-09-10
Category : Science
ISBN : 0199884897

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Searching for reaction in organic synthesis has been made much easier in the current age of computer databases. However, the dilemma now is which procedure one selects among the ocean of choices. Especially for novices in the laboratory, it becomes a daunting task to decide what reaction conditions to experiment with first in order to have the best chance of success. This collection intends to serve as an "older and wiser lab-mate" one could have by compiling many of the most commonly used experimental procedures in organic synthesis. With chapters that cover such topics as functional group manipulations, oxidation, reduction, and carbon-carbon bond formation, Modern Organic Synthesis in the Laboratory will be useful for both graduate students and professors in organic chemistry and medicinal chemists in the pharmaceutical and agrochemical industries.

Author : Reinhard Bruckner
Publisher : Springer Science & Business Media
Page : 873 pages
File Size : 10,6 MB
Release : 2010-01-20
Category : Science
ISBN : 3642036503

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This English edition of a best-selling and award-winning German textbook Reaction Mechanisms: Organic Reactions · Stereochemistry · Modern Synthetic Methods is aimed at those who desire to learn organic chemistry through an approach that is facile to understand and easily committed to memory. Michael Harmata, Norman Rabjohn Distinguished Professor of Organic Chemistry (University of Missouri) surveyed the accuracy of the translation, made certain contributions, and above all adapted its rationalizations to those prevalent in the organic chemistry community in the English-speaking world. Throughout the book fundamental and advanced reaction mechanisms are presented with meticulous precision. The systematic use of red "electron-pushing arrows" allows students to follow each transformation elementary step by elementary step. Mechanisms are not only presented in the traditional contexts of rate laws and substituent effects but, whenever possible, are illustrated using practical, useful and state-of-the-art reactions. The abundance of stereoselective reactions included in the treatise makes the reader familiar with key concepts of stereochemistry. The fundamental topics of the book address the needs of upper-level undergraduate students, while its advanced sections are intended for graduate-level audiences. Accordingly, this book is an essential learning tool for students and a unique addition to the reference desk of practicing organic chemists, who as life-long learners desire to keep abreast of both fundamental and applied aspects of our science. In addition, it will well serve ambitious students in chemistry-related fields such as biochemistry, medicinal chemistry and pharmaceutical chemistry. From the reviews: "Professor Bruckner has further refined his already masterful synthetic organic chemistry classic; the additions are seamless and the text retains the magnificent clarity, rigour and precision which were the hallmark of previous editions. The strength of the book stems from Professor Bruckner’s ability to provide lucid explanations based on a deep understanding of physical organic chemistry and to limit discussion to very carefully selected reaction classes illuminated by exquisitely pertinent examples, often from the recent literature. The panoply of organic synthesis is analysed and dissected according to fundamental structural, orbital, kinetic and thermodynamic principles with an effortless coherence that yields great insight and never over-simplifies. The perfect source text for advanced Undergraduate and Masters/PhD students who want to understand, in depth, the art of synthesis ." Alan C. Spivey, Imperial College London "Bruckner’s ‘Organic Mechanisms’ accurately reflects the way practicing organic chemists think and speak about organic reactions. The figures are beautifully drawn and show the way organic chemists graphically depict reactions. It uses a combination of basic valence bond pictures with more sophisticated molecular orbital treatments. It handles mechanisms both from the "electron pushing perspective" and from a kinetic and energetic view. The book will be very useful to new US graduate students and will help bring them to the level of sophistication needed to be serious researchers in organic chemistry." Charles P. Casey, University of Wisconsin-Madison "This is an excellent advanced organic chemistry textbook that provides a key resource for students and teachers alike." Mark Rizzacasa, University of Melbourne, Australia.

Author : Barry M. Trost
Publisher : Elsevier
Page : 1166 pages
File Size : 37,13 MB
Release : 1992-09-08
Category : Science
ISBN : 0080912516

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This volume contains 37 chapters on methods for reducing functional groups, organized into four main parts. (i) Reduction of C=X systems, where X is an electronegative heteroatom, divided into 14 chapters based on the degree of reduction, the oxidation level of the C=X substrate, and on the nature of the reagent. (ii) Reduction of X=Y systems, divided into three chapters, covering the reduction of such groups as nitro, azo, and the various kinds of P=O and S=O groups. (iii) Reduction of C=C and C≡C, divided into 12 chapters based on the method of reduction, with aromatic, heteroaromatic, and conjugated systems treated separately, and including an extensive discussion of hydrometallation. (iv) Reduction of single bonds, C-X to C-H, in eight chapters, including the hydrogenolysis of the various kinds of C-X bonds, the reduction of epoxides, and the reduction of vinyl derivatives to alkenes. Each chapter includes a discussion of chemoselectivity, regioselectivity, and stereoselectivity, wherever it is appropriate, and most include advice on the reagent of choice, and the mechanistic basis of the various methods of reduction. In short, it is, within the space available, as near to a comprehensive account of reduction in organic chemistry as one could hope for.

Author : Philip L. Fuchs
Publisher : John Wiley & Sons
Page : 640 pages
File Size : 30,69 MB
Release : 2016-07-19
Category : Science
ISBN : 1119279836

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From Boron Trifluoride to Zinc, the 52 most widely used reagents in organic synthesis are described in this unique desktop reference for every organic chemist. The list of reagents contains classics such as N-Bromosuccinimide (NBS) and Trifluoromethanesulfonic Acid side by side with recently developed ones like Pinacolborane and Tetra-n-propylammonium Perruthenate (TPAP). For each reagent, a concise article provides a brief description of all important reactions for which the reagent is being used, including yields and reaction conditions, an overview of the physical properties of the reagent, its storage conditions, safe handling, laboratory synthesis and purification methods. Advantages and disadvantages of the reagent compared to alternative synthesis methods are also discussed. Reagents have been hand-picked from among the 5000 reagents contained in EROS, the Encyclopedia of Reagents for Organic Synthesis. Every organic chemist should be familiar with these key reagents that can make almost every reaction work.

Author : Francis A. Carey
Publisher : Springer Science & Business Media
Page : 1344 pages
File Size : 49,74 MB
Release : 2007-09-06
Category : Medical
ISBN : 038768350X

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The two-part, fifth edition of Advanced Organic Chemistry has been substantially revised and reorganized for greater clarity. The material has been updated to reflect advances in the field since the previous edition, especially in computational chemistry. Part B describes the most general and useful synthetic reactions, organized on the basis of reaction type. It can stand-alone; together, with Part A: Structure and Mechanisms, the two volumes provide a comprehensive foundation for the study in organic chemistry. Companion websites provide digital models for students and exercise solutions for instructors.