Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

McNaught, A., The Nomenclature

R. A. Y. Jones and J. F. Bunnett. Nomenclature for organic chemical transformations (lUPAC Recommendations 1989) , PureAppl. Chem. 61, 725-768 (1989). lUPAC. Compendium of Chemical Terminology, 2nd ed. (the Gold Book ). Compiled by A. D. McNaught and A.Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version http //goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata updates compiled by A. Jenkins. [Pg.249]

In the remaining two chapters in the present volume, L. B. Clapp deals with 1,2,4-oxadiazoles, and A. D. McNaught has tackled the daunting task of explaining the intricacies of heterocyclic nomenclature. [Pg.334]

We thank Dr. A. D. McNaught (Royal Society of Chemistry, London) for advice on nomenclature. We find it convenient to retain the term isoindolenine for general discussion, since it makes a clearer differentiation between the names of the tautomers. However, we have used the alternative term, 1H-isoindole, for systematic nomenclature. We thank the Science Research Council, the Medical Research Council, and Glaxo Group Research Ltd. for support. [Pg.399]


See other pages where McNaught, A., The Nomenclature is mentioned: [Pg.296]    [Pg.336]    [Pg.296]    [Pg.203]    [Pg.288]    [Pg.318]    [Pg.347]    [Pg.347]    [Pg.319]    [Pg.296]    [Pg.296]    [Pg.336]    [Pg.296]    [Pg.203]    [Pg.288]    [Pg.318]    [Pg.347]    [Pg.347]    [Pg.319]    [Pg.296]    [Pg.714]    [Pg.311]    [Pg.535]    [Pg.655]   


SEARCH



A nomenclature

© 2024 chempedia.info