Alcohols, Phenols
-OH
Thiols
-SH
AlcOhOl}
Phenol ates
-OM
Thioalcohol }
.
ates
ThlOphenol
-SM
Amines
-NH2
Imines
=NH
a
C atoms in bold type are included in the stem name.
b
See also radicofunctional nomenclature
C
Formerly: Amidino-, -carboxamidine- and -amidine, respectively.
d
Systematically: amino(sulfonyl, sulfinyl, sulfanyl) ...
Hydroxy ...
. .. 01
Sulfanyl ...
. .. thiol
(Mercapto
... )
M-oxido
...
M ... olate
M-sulfido ...
M ... thiolate
Amino
...
•
b
... amme
Imino ...
. .
b
... Imme
This table
can easily be logically extended. Thus, for example, the naming procedures for sulf(onic, inic, enic) acids and their derivatives are
directly transferable to thio analogues. Several of the characteristic groups presented here can be further substituted in their -NH2 and -OH
functions. In
the respective names this is accounted for by prefixing the corresponding group name including its locant, e.g.: N-methylhexanamide.
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