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Theory of Organic Reactions
  • Language: en
  • Pages: 304

Theory of Organic Reactions

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Advanced Organic Chemistry
  • Language: en
  • Pages: 1216

Advanced Organic Chemistry

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.

Enamines
  • Language: en
  • Pages: 720

Enamines

  • Type: Book
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  • Published: 2017-11-22
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  • Publisher: Routledge

Reviewing and correlating in detail the synthetic, mechanistic, and physical properties ofenamines, this reference features an extensive discussion of all enamine literature ...numerous practical examples of synthetic enamine applications ... new information onoxidation-reduction reactions of enamines ... numerous tables and schemes that givefast, easy access to a wealth of useful data .. . and improved coordination among contributingauthors to reduce duplication and overlap.Thoroughly updating the original edition, Enamines, Second Edition contains over2,400 bibliographic citations that help researchers investigate particular subjects ingreat.er depth. It comprises an authoritative source for organic, synthetic, physical, andnatural products chemists in academe, industry, or government, as well as for advancedgraduate students in these disciplines.

Unified Valence Bond Theory of Electronic Structure
  • Language: en
  • Pages: 598

Unified Valence Bond Theory of Electronic Structure

The bond diagrammatic representation of molecules is the foundation of MOVB theory. To a certain extent, this kind of representation is analogous to the one on which "resonance theory" is based and this fact can be projected by a comparison of the various ways in which MOVB theory depicts a species made up of three core and two ligand MO's which define two subsystems containing a total of six electrons and the ways in which "resonance theory" (i. e. , qualitative VB theory) depicts a six-electron-six-AO species such as the pi system of CH =CH-CH=CH-CH=O. The 2 different pictorial representations are shown in Scheme 1 so that the analogies are made evident. First of all, the total MOVB diagra...

Topics in Stereochemistry
  • Language: en
  • Pages: 550

Topics in Stereochemistry

This seminal series, first edited by Ernest Eliel, responsible for some of the major advances in stereochemistry and the winner of the ACS Priestley Medal in 1996, provides coverage of the major developments of the field of stereochemistry. The scope of this series is broadly defined to encompass all fields of chemical and biological sciences that are founded on molecular and supramolecular interactions. Insofar as chemical, physical, and biological properties are determined by molecular shape and structure, the importance of stereochemistry is fundamental to and consequential for all natural sciences. Topics in Stereochemistry serves as a multidisciplinary series that enriches all of chemis...

Advances in Physical Organic Chemistry APL
  • Language: en
  • Pages: 271

Advances in Physical Organic Chemistry APL

Advances in Physical Organic Chemistry APL

Organic Reaction Mechanisms 1973 Reprint A
  • Language: en
  • Pages: 590

Organic Reaction Mechanisms 1973 Reprint A

The only book series to summarize the latest progress on organic reaction mechanisms, Organic Reaction Mechanisms, 1973 surveys the development in understanding of the main classes of organic reaction mechanisms reported in the primary scientific literature in 1973. The 9th annual volume in this highly successful series highlights mechanisms of stereo-specific reactions. Reviews are compiled by a team of experienced editors and authors, allowing advanced undergraduates, graduate students, postdocs, and chemists to rely on the volume's continuing quality of selection and presentation.

Progress in Physical Organic Chemistry
  • Language: en
  • Pages: 376

Progress in Physical Organic Chemistry

Progress in Physical Organic Chemistry is dedicated to reviewing the latest investigations into organic chemistry that use quantitative and mathematical methods. These reviews help readers understand the importance of individual discoveries and what they mean to the field as a whole. Moreover, the authors, leading experts in their fields, offer unique and thought-provoking perspectives on the current state of the science and its future directions. With so many new findings published in a broad range of journals, Progress in Physical Organic Chemistry fills the need for a central resource that presents, analyzes, and contextualizes the major advances in the field. The articles published in Pr...

New Theoretical Concepts for Understanding Organic Reactions
  • Language: en
  • Pages: 403

New Theoretical Concepts for Understanding Organic Reactions

People who attended the NATO Advanced Study Institute (ASI) entitled NEW THEORETICAL CONCEPTS FOR UNDERSTANDING ORGANIC REAC TIONS held at Sant Feliu de Gufxols on the Costa Brava of Spain had a unique experience. They have seen the evolution of the field from qualitative arguments through the generation of Potential Energy Surfaces (PES) to the use of PES in molecular dynamics. The excellent lectures that were dedicated to the various aspects of Potential Energy Surfaces clearly revealed a colossal amount of ma terial that represents our current understanding of the overall problem. It is our hope that the present volume will recreate the excitement in the readers that we all experienced du...

Organolithiums
  • Language: en
  • Pages: 408

Organolithiums

  • Type: Book
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  • Published: 2002-07-12
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  • Publisher: Elsevier

Organolithiums: Selectivity for Synthesis.