ISBN: 3540411380
TITLE: Systematic Nomenclature of Organic Chemistry
AUTHOR: Hellwinkel, Dieter
TOC:

Introduction
Literature
1 Parent Structures
1.1 Acyclic Hydrocarbon Systems
1.1.1 Linear Systems
1.1.2 Branched Systems
1.1.3 Systems with Branched Side Chains
1.1.4 Multivalent Substituent Groups
1.2 Cyclic Systems
1.2.1 Cyclic Hydrocarbon Systems
1.2.1.1 Monocyclic Hydrocarbons
1.2.1.2 Polvcyclic Hydrocarbons
1.2.1.2.1 Fused Polycyclic Hydrocarbons
1.2.1.2.2 Bridged Polycyclic Hydrocarbons
1.2.1.2.2.1 von Baeyer System
1.2.1.2.2.2 Bridged Fused Systems
1.2.1.2.3 Spirocyclic Hydrocarbon Systems
1.2.1.2.4 Hydrocarbon Ring Systems Linked through Single or Double Bonds; Ring Assemblies
1.2.1.2.5 Cyclic Hydrocarbons with Side Chains
1.2.2 Heterocyclic Systems
1.2.2.1 Trivialnames
1.2.2.2 Replacement Nomenclature
1.2.2.3 The Hantzsch-Widman System
1.2.2.4 Fused Heterocyclic Systems
1.3 Phane Nomenclature
1.3.1 Cyclophanes
1.3.2 Other Phanes
2 Substituted Systems
2.1 Preliminary General Remarks
2.2 Nomenclature Types for Substituted Systems
2.2.1 Substitutive Nomenclature
2.2.2 Functional Class Names (Formerly: Radiofunctional Nomenclature)
2.2.3 Additive Nomenclature
2.2.4 Subtractive Nomenclature
2.2.5 Conjunctive Nomenclature
2.2.6 Naming of Substituted Assemblies of Identical Units
2.2.6.1 Components with direct Linkage
2.2.6.2 Identical Components Bound to Di- or Polyvalent Groups
2.2.7 Naming of Radical and Ionic Species
2.2.7.1 Free Radicals
2.2.7.2 Cations
2.2.7.3 Radical Cations (Cation Radicals)
2.2.7.4 Anions
2.2.7.5 Radio Alanions (Anion Radicals)
2.2.7.6 Compounds with two (are more) Identcally Charged Centers
2.2.7.7 Compounds with Positively and Negatively Charged Centers (Zwitterions)
3 Prief Demonstration of the General Nomenclature Rules for the Most Important Traditional Compound Classes (Functional Parents)
3.1 Carboxylic Acids, Sulfonic Acids etc. and their derivatives
3.2 Nitrile, isocyanides and similar compounds
3.3 Aldehydes and Ketones
3.4 Alcohols, Phenols and their Derivatives
3.5 Ethers and Thioethers
3.6 Amines, Imines and their Derivatives
3.7 Halogen Derivatives
3.8 Compounds with Nitrogen Chains
3.8.1 Azo- and Azoxy Compounds
3.9 Hydrazines and their Derivatives
3.10 Diazo- and Diazonium Compounds
3.11 Compounds with Chains of Three or More Nitrogen Atoms
3.12 Other Polynitrogen Parent Systems
4 Metalorganic and Metalloidorganic Compounds
4.1 Element Hydride (Elementane) Names
4.2 Functionaly Substituted Elementanes
4.3 Elementanes with Repeating Diads
4.4 Organic Derivatives of Alkali and Alkaline Earth Metals and Comparable Compounds
4.5 "ate" Complexes
5 Carbohydrates
5.1 Aldoses
5.2 Ketoses
5.3 Ketoaldoses (Aldoketoses, Aldosuloses)
5.4 Deoxy Sugars
5.5 Amino Sugars and Analogously Substituted Derivatives
5.6 Transformations of Carbonyl Functions
5.6.1 Oximes, Hydrazones, Osazones
5.6.2 Acetals, Ketals etc.
5.7 Branched Sugars
5.8 Sugar Alcohols (Alditols)
5.9 Acids Derived from Sugars
5.10 O-Substitution
5.10.1 O-Substitution with Alkyl- and Acylgroups
5.10.2 Cyclic Acetals and Ketals
5.11 Monosaccharides as Substituent Groups
5.12 Glycosides and Glycosyl-Compounds
5.12.1 Glycosides
5.12.2 Glycosyl Compounds
5.13 Oligosaccharides
5.13.1 Oligosaccharides with Free Hemiacetal Group
5.13.2 Oligosaccharidea withot Free Hemiacetal Group
5.13.3 Polysaccharides (Glycans)
5.14 Customary Trivial Names
6 Construction of the Names of Complex Compounds
6.1 Determination of the Highest Ranked Chain (Main or Senior Chain)
6.2 Determination of the Most Senior Ring System
6.3 Treatment of the Most Senior Characteristic Group in the Ligh of the Two Preceding Paragraphs
6.4 Numbering
6.5 Order of Prefixes
6.6 Isotopically Modified Compounds
6.7 Specifications of Stereochemistry
6.7.1 cis/trans Isomerism; The Z/E-Convention
6.7.1.1 Double Bond Systems
6.7.1.2 Ring Systems
6.7.2 Specification of Absolute and Relative Configuration
6.7.2.1 Compounds with Stereogenic (Traditionally Symmetric) Carbon (and Analogous) Centers
6.7.2.2 Compounds with Helical Stereogenic Units
6.7.2.2.1 Screw-like Molecules (One Chirality Axis)
6.7.2.2.2 Propeller-Molecules (Several Chirality Axes)
6.7.2.3 Molecules Exhibiting Planar Chirality
6.7.3 Concluding Remarks
7 Appendix
7.1 Complete List of "a" Terms Utilized in Replacement and Heterane Nomenclature
7.2 Tables of Customary Trivial (and Semitrivial) Names
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