Alicyclic Compounds - 2nd Edition - ISBN: 9780444898449, 9781483144603

Alicyclic Compounds

2nd Edition

Monocarbocyclic Compounds to and Including Five Ring Atoms, Six- and Higher-Membered Monocarbocyclic Compounds (Partial: Chapter 5 in This Volume)

Editors: Malcolm Sainsbury
eBook ISBN: 9781483144603
Imprint: Elsevier
Published Date: 4th December 1992
Page Count: 540
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Description

Rodd's Chemistry of Carbon Compounds, Volume II: Alicyclic Compounds surveys advances in the chemistry of three- to six-membered monocarbocycles from 1973 to 1991. This book begins with a detailed review of the conformations and stereochemical analyses of alicycles, including higher members of the series, and then proceeds to deal with the chemistry of individual ring systems. The next chapters cover the prostaglandins and their allies and natural products bearing a cyclohexane, cyclohexene, or cyclohexadiene ring system. A review of the chemistry of the cyclohexadienes and their metallic complexes is provided at the end. This text also includes a list of common abbreviations and symbols. This volume benefits chemical engineering students, particularly those studying the components of organic chemicals.

Table of Contents


Preface

List of Common Abbreviations and Symbols Used

Chapter 1. Alicyclic Hydrocarbons, Conformation and Stereochemistry

1. Introduction

2. Three-Membered Rings

(a) Cyclopropanes with Unsaturated Substituents

(b) Cyclopropanes with Saturated Substituents

3. Four-Membered Rings

(a) Cyclobutanes

(b) Monosubstituted Cyclobutanes

(c) Disubstituted Cyclobutanes

(d) Unsaturated Four-Membered Ring Carbocycles

(e) Cyclobutanones

4. Five-Membered Rings

(a) Cyclopentane

(b) Cyclopentene

(c) Cyclopentanone

5. Six-Membered Rings

(a) Cyclohexane

(b) Monosubstituted Cyclohexanes

(c) 1,1-Disubstituted Cyclohexanes

(d) 1,2-Disubstituted Cyclohexanes

(e) 1,1,2-Trisubstituted Cyclohexanes

(f) 1,3- and 1,3,5-Substituted Cyclohexanes

(g) 1,4-Disubstituted Cyclohexanes

(h) Sterically Crowded Cyclohexanes

(i) Cyclohexene

(j) 1,3-Cyclohexadiene

(k) 1,4-Cyclohexadienes

(l) Exomethylenecyclohexane

(m)Cyclohexanones, Cyclohexanediones and Cyclohexenones

6. Seven-Membered Rings

(a) Cycloheptanes

(b) Cycloheptanones

(c) Cycloheptene and Cycloheptene Oxide

(d) Cyeloheptadienes and Cycloheptatrienes

7. Eight-Membered Rings

(a) Cyclooctanes

(b) Cyclooctanones

(c) Cyclooctene, Cyclooctyne and 1,2-Cyclooctadiene

(d) 1,3-, 1,4- and 1,5-Cyclooctadienes

(e) Cyclooctatrienes

8. Nine-Membered Rings

(a) Cyclononane, Cyclononanone and Cyclononyne

(b) 1,2-Cyclononadiene and 1,5-Cyclononadiene

(c) Cyclononatrienes

9. Ten-Membered Rings

10. Ring Systems Larger than Ten-Membered

Chapter 2. The Cyclopropanes

1. Introduction

2. Preparation of Cyclopropanes

(a) Intramolecular Nucleophilic Substitution

(b) Simmons-Smith Reaction

(c) Reaction of Alkenes with Diazo Compounds

(d) Reaction of Alkenes with Dihalocarbenes and Other Carbenoids

(e) Ring Contraction of Cyclobutanes

(F) Reactions of Electron Deficient Carbon-Carbon Double Bonds with Phosphoranes, Sulfuranes and Arsenic Ylides

(G) Photochemical Reaction

(H) Radical Mediated Reaction

(I) Organometallic Reaction

(J) Miscellaneous Reaction

3. Use of Cyclopropanes in Organic Synthesis

(a) Thermal Ring Fission

(b) Reductive and Oxidative Ring Fission

(c) Electrophilic and Nucleophilic Ring Fission

(d) Radical Mediated Ring Fission

(e) Metal Salt Mediated Ring Fission

Chapter 3. The Cyclobutanes

1. Introduction, Structure, Properties, and Theoretical Considerations

2. Synthesis of the Cyclobutane Ring System

(a) [2+2] Cycloaddition Reactions

(b) Intramolecular Cyclisations

(c) Ring Expansion Reactions

(d) Ring Contractions

3. Reactions of Cyclobutanes

(a) Solvolyses and Rearrangements of Cyclobutanes and Cyclobutenes

(b) Electrocyclic Ring Opening-Ring Closing Reactions

(c) Miscellaneous Reactions of Cyclobutanes and Cyclobutenes

(d) Reactions of Cyclobutanols, Cyclobutanones and Cyclobutenones

(e) Reactions of Cyclobutenenitriles

(F) Reactions of Squaric and Semisquaric Acids

Chapter 4a. The Cyclopentanes

1. Reviews, Theoretical and Structural Aspects, General Properties

2. Synthesis

(a) Cyclisation Reactions Leading to Cyclopentanes, Cyclopentenes; General Cyclopentane Ring Synthesis

(b) Cyclopentanes and Cyclopentenes by Cycloaddition Reactions

(c) Cyclopentanes and Cyclopentenes by Ring Expansion and Ring Contraction Processes

(d) Cyclopentanones and Cyclopentenones by Cyclisation Processes

(e) Cyclopentanones and Cyclopentenones by Cycloaddition Reactions

(F) Cyclopentanones and Cyclopentenones by Ring Expansion and Ring Contraction Reactions

(G) Cyclopentanones and Cyclopentenones by Rearrangements and by Miscellaneous Reactions

3. Reactions

(a) Cyclopentanes, Cyclopentenes, and Simple Derivatives

(b) Cyclopentanones, Cyclopentenones, and Derivatives

Chapter 4b. Natural Products Containing the Cyclopentane Sub-Unit: Prostaglandins

1. Introduction

2. Structure and Nomenclature

3. Prostaglandin Biosynthesis

(a) Mammalian Biosynthesis

(b) Non-Mammalian Biosynthesis

4. Prostaglandin Total Synthesis

(a) Corey's Bicyclic Lactone Approach

(b) Approaches via Polycyclic Intermediates

(c) Conjugate Addition and Three Component Coupling Approaches

(d) Recent Synthetic Approaches to PGs

(e) PG Metabolism and Analogue Synthesis

(F) Synthesis of Non-mammalian Prostanoids

5. Bibliography

(a) General and Biological

(b) Synthetic

Chapter 4c. Cyclopentadiene

1. Introduction

2. Preparation of σ-Bonded Cyclopentadiene Derivatives

(a) Deuteriated Cyclopentadiene

(b) Alkyl Substituents

(c) Cyano, Carbonyl, Carboxyl and Trifluoromethyl Substituents

(d) Phosphine Substituents

(e) Other Substituents

3. Ionic Metal Derivatives

4. Fluxionality of Cyclopentadienyl Derivatives

5. Metal Complexes - Structure and Reactions

(a) The Cyclopentadienyl Ligand

(b) Monoligating Cyclopentadienyl Complexes

(c) Bridged Biscyclopentadiene Complexes

(d) Bifunctional Cyclopentadienyl Ligands

6. Metal Complexes - Applications

7. Reactions of Cyclopentadiene

Chapter 5a. Cyclohexane and Its Derivatives

Introduction

1. Cyclohexane

(a) Synthesis

2. Halogenocyclohexanes

(a) Fluorocyclohexane and Derivatives

(b) Chlorocyclohexane

(c) Bromocyclohexane

(d) Halogenocyclohexanes through Addition to Benzene Rings

3. Cyclohexadienyl Intermediates

(a) Cyclohexadienyl Radical

(b) Muonium Attack

(c) Cyclohexadienylium Ion

4. Cyclohexanol and Cyclohexanone

(a) Synthesis

5. Cyclohexadienones and Derivatives

(a) Identification and Preparation

6. Cyclohexanamine (Cyclohexylamine)

Chapter 5b. Natural Products Containing a Cyclohexane, Cyclohexene, or Cyclohexadiene Subunit

1. Simple Examples

(a) Nonfunctionalized

(b) Functionalized

2. Nonfunctionalized or Unusual Terpenoids

(a) Mono Terpenoids

(b) Nonfunctionalized Sesquiterpenes

(c) Norsesquiterpenes

(d) Furanoterpenes

(e) Oxygenated Norterpenoids

(F) Rearranged or Unusual Terpenoids

3. C13 Norterpenoids

4. Flavonoid, Chalcone, and Coumarin Types

5. Shikimic Acid Pathway

(a) Mechanistic Aspects

(b) Synthesis

(c) Natural Occurrence

6. Cyclitols

(a) Natural Occurrence

(b) Synthesis

(c) Cyclitol Epoxides

7. Inositols

(a) Natural Occurrence

(b) Synthesis

8. Pseudosugars

(a) Natural Occurrence

(b) Synthesis

9. Aminocyclitols

(a) Natural Occurrence

(b) Synthesis

10. Benzoquinones

11. Quinols

12. Halogenated Tyrosine Metabolites

13. Concluding Remarks

Chapter 5c. Cyclohexadienes

1. Introduction

2. Preparation of Cyclohexadienes

(a) Metal-Ammonia (Birch) Reduction of Aromatic Compounds

(b) Microbial Oxidation of Aromatic Compounds

(c) Cyclohexadienes from Cyclohexenones

3. Reactions of Cyclohexadienes

(a) Conjugation of 1,4-Cyclohexadienes

(b) Cycloaddition Reactions

(c) Palladium-Catalyzed 1,4-Difunctionalization

4. Metal Complexes of Cyclohexadienes

(a) Cyclohexadiene-Fe(CO)2L Complexes

(b) Cyclohexadiene-CoCp Complexes and the Derived Cyclohexadienyl-CoCp Cations

(c) Cyclohexadiene-Mo(CO)2Cp and Related Complexes

Guide to the Index

Index


Details

No. of pages:
540
Language:
English
Copyright:
© Elsevier 1992
Published:
Imprint:
Elsevier
eBook ISBN:
9781483144603

About the Editor

Malcolm Sainsbury