Systematic Nomenclature of Organic, Organometallic and Coordination Chemistry. Chemical-Abstracts Guidelines with IUPAC Recommendations and Many Trivial Names
Ursula Bünzli-Trepp
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Ursula Bünzli-Trepp, Systematic Nomenclature of Organic, Organometallic and Coordination Chemistry. Chemical-Abstracts Guidelines with IUPAC Recommendations and Many Trivial Names (2021), Logos Verlag, Berlin, ISBN: 9783832585389
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Beschreibung / Abstract
This second English edition has been revised and upgraded to contain the latest Chemical-Abstracts and IUPAC nomenclature guidelines. The book is aimed at chemists, biochemists, pharmacologists, scientists at all levels in academia and industry, as well as documentalists, editors, and software developers. It presents in a user-friendly way all that is required to construct or interpret systematic names of organic, organometallic, and coordination compounds, including those of more complicated molecules:
-Logic, coherent structure and organization of the material according to the procedure of naming, based on the most recent Chemical-Abstracts nomenclature guidelines, with references to the 2013 recommendations for IUPAC-preferred names (PINs) and with many trivial names.
- Detailed description of the names of molecular-skeleton parents, including an illustrative procedure for the naming of fused polycycles.
- Construction of the names of all compound classes illustrated by colors, with an emphasis on radicals, ions, and organometallic and coordination compounds.
- Collection of the stereoparent names of the alkaloids, amino acids, peptides, carbohydrates, cyclitols, nucleosides, nucleotides, nucleic acids, steroids, terpenes, carotenoids, retinoids, vitamins, and prophyrins as well as guidelines for the naming of polymers and isotopically modified compounds.
- Detailed instructions for the citation of indicated H atom (indicated hydrogen) in names and naming of tautomers.
- Comprehensive description of the Cahn--Ingold--Prelog system for the specification of configuration and of the thus derived stereodescriptors for names of chiral organic, organometallic, and coordination compounds, including instructions concerning the stereodescriptors used by Chemical Abstracts until 1999.
- Over 6000 drawings of compounds with names from practice, about 3000 in color.
-Logic, coherent structure and organization of the material according to the procedure of naming, based on the most recent Chemical-Abstracts nomenclature guidelines, with references to the 2013 recommendations for IUPAC-preferred names (PINs) and with many trivial names.
- Detailed description of the names of molecular-skeleton parents, including an illustrative procedure for the naming of fused polycycles.
- Construction of the names of all compound classes illustrated by colors, with an emphasis on radicals, ions, and organometallic and coordination compounds.
- Collection of the stereoparent names of the alkaloids, amino acids, peptides, carbohydrates, cyclitols, nucleosides, nucleotides, nucleic acids, steroids, terpenes, carotenoids, retinoids, vitamins, and prophyrins as well as guidelines for the naming of polymers and isotopically modified compounds.
- Detailed instructions for the citation of indicated H atom (indicated hydrogen) in names and naming of tautomers.
- Comprehensive description of the Cahn--Ingold--Prelog system for the specification of configuration and of the thus derived stereodescriptors for names of chiral organic, organometallic, and coordination compounds, including instructions concerning the stereodescriptors used by Chemical Abstracts until 1999.
- Over 6000 drawings of compounds with names from practice, about 3000 in color.
Beschreibung
Ursula B ünzli-Trepp (b. 1943) obtained her diploma in chemistry in 1967 at the Swiss Federal Institute of Technology Z ürich (ETH-Z), with a diploma thesis in synthetic organic chemistry performed under the supervision of Prof. D. Arigoni. She received her Ph.D. at the Ecole polytechnique fédérale de Lausanne (EPFL) in 1971 under the auspices of Prof. H. Dahn and Prof. H. Moll, with a thesis on reaction mechanisms in organic chemistry. From 1971 to 1973, she did postdoctoral work in the field of alkaloid synthesis with Prof. J.P. Kutney at the University of British Columbia in Vancouver, Canada. After another year at ETH-Z as scientific collaborator of Prof. O. Jeger, she joined the editorial office of the journal Helvetica Chimica Acta in 1975 where she was active as an Assistant Editor until 2013. Ursula B ünzli-Trepp is a member of the Advisory Subcommittee of IUPAC's Division of Chemical Nomenclature and Structure Representation.
Inhaltsverzeichnis
- BEGINN
- 1 Directions for Use of the Book
- 2 Fundamentals
- 2.1 Nomenclature terms and definitions used in the Book
- 2.2 Conventions for enclosing marks and vowels in names
- 3 Guide to Name Construction and Name Interpretation
- 3.1 General procedure and choice of the senior compound class (choice of the principal group)
- 3.2 Nomenclature types
- 3.3 Determination of the molecular-skeleton parent
- 3.4 Numbering of the molecular-skeleton parent and of other structure components
- 3.5 Alphabetical order of prefixes or parent-substituent names
- 4 Molecular-Skeleton Parents
- 4.1 Preliminary notes
- 4.2 Hydrocarbon chains
- 4.3 Heterochains
- 4.4 Carbomonocycles
- 4.5 Heteromonocycles
- 4.6 Fused polycycles (carbo- and heterocycles)
- 4.7 von Baeyer bridged polycycles (carbo- and heterocycles)
- 4.8 Bridged fused polycycles (carbo- and heterocycles)
- 4.9 Spiropolycycles (carbo- and heterocycles)
- 4.10 Ring assemblies of identical ring components (carbo- and heterocycles)
- 5 Substituent Prefixes
- 5.1 Preliminary notes
- 5.2 Prefixes of mononuclear substituents
- 5.3 Prefixes of hydrocarbon-chain substituents
- 5.4 Prefixes of heterochain substituents
- 5.5 Prefixes of carbocycle substituents
- 5.6 Prefixes of heterocycle substituents
- 5.7 Prefixes of ring-assembly substituents
- 5.8 Prefixes of composite substituents: choice of the parent substituent
- 5.9 Prefixes of carbonyl-containing substituents and analogs
- 6 Compound Classes
- 6.1 Preliminary notes
- 6.2 Radicals
- 6.3 Cations
- 6.4 Anions
- 6.5 Zwitterions
- 6.6 Radical ions
- 6.7 Carboxylic, carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, carboximidic, and corresponding carboperoxoic acids and salts
- 6.8 Sulfonic, sulfinic, and sulfenic acids, selenonic, seleninic, and selenenic acids, telluronic, tellurinic, and tellurenic acids, their chalcogeno, hydrazono, imido, and peroxy replacement analogs, and corresponding salts
- 6.9 C-Oxoacids: carbonic and formic acid and their replacement analogs and corresponding salts
- 6.10 S-, Se-, Te-, and N-Oxoacids
- 6.11 P- and As-Oxoacids
- 6.12 Sb-, Bi-, Si-, and B-Oxoacids
- 6.13 Anhydrides
- 6.14 Esters and lactones
- 6.15 Acid halides
- 6.16 Amides, lactams, cyclic imides, and amidines
- 6.17 Hydrazides
- 6.18 Nitriles
- 6.19 Aldehydes and their oxime and hydrazone derivatives
- 6.20 Ketones and their oxime and hydrazone derivatives
- 6.21 Alcohols and phenols
- 6.22 Hydroperoxides
- 6.23 Amines
- 6.24 Imines
- 6.25 Nitrogen compounds
- 6.26 Phosphorus and arsenic compounds
- 6.27 Antimony and bismuth compounds
- 6.28 Boron compounds
- 6.29 Silicon, germanium, tin, and lead compounds
- 6.30 Oxygen compounds
- 6.31 Sulfur, selenium, and tellurium compounds
- 6.32 Carbon compounds
- 6.33 Halogen compounds
- 6.34 Organometallic and coordination compounds
- Appendixes
- A.1 Specialist nomenclatures
- A.2 Multiplying affixes
- A.3 Modifying syllables
- A.4 Heteroatom syllables and element names
- A.5 Indicated H atom 'H ' (indicated hydrogen) and tautomers
- A.6 Configuration descriptors in names
- A.7 Lambda (λ) convention
- A.8 Isotopically modified compounds
- A.9 List of substituent prefixes
- Index