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Amides and Imides

Monoacylamines Rule C-823

823.1 - (a) Names of radicals , , , etc., formed by loss of a hydrogen atom from the NH2 or NHR group of an amide, are derived from the systematic or semi-trivial name of the amide by changing the ending "-amide" to "-amido-", such radical names being used when the compound contains also a group having priority for citation as principal group. (b) Alternatively the radicals are named as acylamino radicals.

Examples to Rule C-823.1

823.2 - Despite Rule C-823.1, radicals derived from amino acids that have trivial names are named only as acylamino radicals, the acyl radical names for the groups being used (see Rule C-421).

Example to Rule C-823.2

See Recommendations'93 R-5.7.8

Next:
Amides and Imides C-824, C-825, C-826, C-827
Nitriles, Isocyanides, and Their Derivatives C-831, C-832, C-833, C-834
Hydroxylamines and Related Compounds C-841, C-842, C-843
Nitroso and Nitro Compounds C-851, C-852
Amine Radical Ions C-861

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This HTML reproduction of Sections A, B and C of IUPAC "Blue Book" is as close as possible to the published version [see Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H, Pergamon Press, Oxford, 1979. Copyright 1979 IUPAC.] If you need to cite these rules please quote this reference as their source.

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