A Quantitative Survey of Steric, Solvation, and Stereoelectronic Effects in Cyclic Organic Molecules
Title | A Quantitative Survey of Steric, Solvation, and Stereoelectronic Effects in Cyclic Organic Molecules PDF eBook |
Author | Miles Andrew Fabian |
Publisher | |
Pages | 466 |
Release | 1996 |
Genre | |
ISBN |
American Doctoral Dissertations
Title | American Doctoral Dissertations PDF eBook |
Author | |
Publisher | |
Pages | 896 |
Release | 1995 |
Genre | Dissertation abstracts |
ISBN |
Advanced Organic Chemistry
Title | Advanced Organic Chemistry PDF eBook |
Author | Francis A. Carey |
Publisher | Springer Science & Business Media |
Pages | 1216 |
Release | 2007-06-27 |
Genre | Science |
ISBN | 0387448993 |
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 A covers fundamental structural topics and basic mechanistic types. It can stand-alone; together, with Part B: Reaction and Synthesis, the two volumes provide a comprehensive foundation for the study in organic chemistry. Companion websites provide digital models for study of structure, reaction and selectivity for students and exercise solutions for instructors.
Stereoelectronic Effects in Organic Chemistry
Title | Stereoelectronic Effects in Organic Chemistry PDF eBook |
Author | Pierre Deslongchamps |
Publisher | Pergamon |
Pages | 396 |
Release | 1983 |
Genre | Science |
ISBN |
Computational Organic Chemistry
Title | Computational Organic Chemistry PDF eBook |
Author | Steven M. Bachrach |
Publisher | John Wiley & Sons |
Pages | 653 |
Release | 2014-04-07 |
Genre | Science |
ISBN | 1118291921 |
The Second Edition demonstrates how computational chemistry continues to shed new light on organic chemistry The Second Edition of author Steven Bachrach’s highly acclaimed Computational Organic Chemistry reflects the tremendous advances in computational methods since the publication of the First Edition, explaining how these advances have shaped our current understanding of organic chemistry. Readers familiar with the First Edition will discover new and revised material in all chapters, including new case studies and examples. There’s also a new chapter dedicated to computational enzymology that demonstrates how principles of quantum mechanics applied to organic reactions can be extended to biological systems. Computational Organic Chemistry covers a broad range of problems and challenges in organic chemistry where computational chemistry has played a significant role in developing new theories or where it has provided additional evidence to support experimentally derived insights. Readers do not have to be experts in quantum mechanics. The first chapter of the book introduces all of the major theoretical concepts and definitions of quantum mechanics followed by a chapter dedicated to computed spectral properties and structure identification. Next, the book covers: Fundamentals of organic chemistry Pericyclic reactions Diradicals and carbenes Organic reactions of anions Solution-phase organic chemistry Organic reaction dynamics The final chapter offers new computational approaches to understand enzymes. The book features interviews with preeminent computational chemists, underscoring the role of collaboration in developing new science. Three of these interviews are new to this edition. Readers interested in exploring individual topics in greater depth should turn to the book’s ancillary website www.comporgchem.com, which offers updates and supporting information. Plus, every cited article that is available in electronic form is listed with a link to the article.
Side Reactions in Organic Synthesis
Title | Side Reactions in Organic Synthesis PDF eBook |
Author | Florencio Zaragoza Dörwald |
Publisher | John Wiley & Sons |
Pages | 389 |
Release | 2006-03-06 |
Genre | Science |
ISBN | 3527604987 |
Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reactivity relationship of organic compounds. This textbook highlights the competing processes and limitations of the most important reactions used in organic synthesis. By allowing chemists to quickly recognize potential problems this book will help to improve their efficiency and success-rate. A must for every graduate student but also for every chemist in industry and academia. Contents: 1 Organic Synthesis: General Remarks 2 Stereoelectronic Effects and Reactivity 3 The Stability of Organic Compounds 4 Aliphatic Nucleophilic Substitutions: Problematic Electrophiles 5 The Alkylation of Carbanions 6 The Alkylation of Heteroatoms 7 The Acylation of Heteroatoms 8 Palladium-Catalyzed C-C Bond Formation 9 Cyclizations 10 Monofunctionalization of Symmetric Difunctional Substrates
The Anomeric Effect
Title | The Anomeric Effect PDF eBook |
Author | Eusebio Juaristi |
Publisher | CRC Press |
Pages | 248 |
Release | 1994-10-12 |
Genre | Science |
ISBN | 9780849389412 |
This book provides a comprehensive review of the structural, conformational, and chemical manifestations of the anomeric effect. In order to present a cogent discussion of this most fundamental and relevant phenomenon, three chapters examine our present understanding of the origin of this conformational effect, based upon a wealth of theoretical and physical data. Equally important, however, are three additional chapters that deal with the general consequences of the stereoelectronic interactions that are associated with the basis of the anomeric effect. The remainder of the book is devoted to new areas of development in the topic-such as differentiation of the endo and exo anomeric interactions, specific analysis of the enthalpic component of anomeric effects, critical evaluation of the kinetics and reverse anomeric effects, discovery of a new substantial effect in second- and lower-row anomeric segments, and others.