222
EIZ convention 186
element hydrides 10 1, 146
elementanes 146,147
elementanes with repeating diads 149
enantiomers 192
endolexo 192
-endo-cydo 34
... ene 12,15,32,33,88
... eno 15,32,33
... enylene 12
epi 34
epithio 57
epoxides 86, 131
epoxy ... 131
erythro/threo 191
esters 116, 118
esters of hyponitrous acid 139
ethers 130, 217
exceptional numbering 200
extended cisltrans formalism 188
Fischer projection 156,157
formal di-, tetra-, etc. hydrogenation
123
formal dihydrogenation 36,104,107
four-point figures 193
free radicals 96, 97
free valences 8,11-13,28,183
functional class 75
functional class nomenclature 115
functional class (radicofunctional)
names 84,85,121
functional class designations 120
functional compound classes 149
functional groups 75,112,149,178,180,
181
functional parents 112
functionally substituted elementanes
149
fused heterocyclic systems 57
fused heterospirocycles 64
fused polycycles 31,38
fused polycyclic hydrocarbons 14
fused systems 22
-, bridged 32,34,65
-, as bridges 34,67
-, carbocyclic 14-28,31
-, heterocyclic 57 ff.
-, hydrogenated 27,85
-, spirocydic 36,38,64
-, as substituent groups 28
fusion locants 21,62
fusion nomenclature 68
fusion positions 24,61
fusion prefixes 15
fusion principles 60
fusion term 34
Subject Index
general chemical terminology 4
glycans 175
glycosides 170
glycosyl compounds 170, 172
graphical conventions 190
graphical representation 22
Grignard compounds 152
group names 76
halogen compounds 218
halogen derivatives 86,137
Hantzsch-Widman system 53-55,57
Haworth representations 157
helical stereogenic units 193,197
helicenes 24,25,193
helicity descriptor 194
helicity symbols 193
(hemi)acetals 163
(hemi)ketals 163
hemialdehydes 115
hemiamides 115
heteranes 146, 148
hetero atoms at fusion positions 51,61
hetero bridges 65
heterocyclic systems 43
-, acylated 135
-, bridged 65-67
-, cationic 63, 103
-, exceptional names for benzo bicycles
60
-, fused 57 - 64
-, fused spirocyclic 64
-, Hantzsch-Widman names 54-57
-,linked 64
-, peripheral (final) numbering 61
-, priorities (seniorities) 57 - 60
-, replacement names 51- 54,64,67
-, trivial names 43-51
heteromonocyclic systems 53
higher membered rings 22
higher order components 21, 26
history of organic chemical nomenclature 4
homo 87,89,204
hydrazides 142
hydrazines 141
EIZ convention 186
element hydrides 10 1, 146
elementanes 146,147
elementanes with repeating diads 149
enantiomers 192
endolexo 192
-endo-cydo 34
... ene 12,15,32,33,88
... eno 15,32,33
... enylene 12
epi 34
epithio 57
epoxides 86, 131
epoxy ... 131
erythro/threo 191
esters 116, 118
esters of hyponitrous acid 139
ethers 130, 217
exceptional numbering 200
extended cisltrans formalism 188
Fischer projection 156,157
formal di-, tetra-, etc. hydrogenation
123
formal dihydrogenation 36,104,107
four-point figures 193
free radicals 96, 97
free valences 8,11-13,28,183
functional class 75
functional class nomenclature 115
functional class (radicofunctional)
names 84,85,121
functional class designations 120
functional compound classes 149
functional groups 75,112,149,178,180,
181
functional parents 112
functionally substituted elementanes
149
fused heterocyclic systems 57
fused heterospirocycles 64
fused polycycles 31,38
fused polycyclic hydrocarbons 14
fused systems 22
-, bridged 32,34,65
-, as bridges 34,67
-, carbocyclic 14-28,31
-, heterocyclic 57 ff.
-, hydrogenated 27,85
-, spirocydic 36,38,64
-, as substituent groups 28
fusion locants 21,62
fusion nomenclature 68
fusion positions 24,61
fusion prefixes 15
fusion principles 60
fusion term 34
Subject Index
general chemical terminology 4
glycans 175
glycosides 170
glycosyl compounds 170, 172
graphical conventions 190
graphical representation 22
Grignard compounds 152
group names 76
halogen compounds 218
halogen derivatives 86,137
Hantzsch-Widman system 53-55,57
Haworth representations 157
helical stereogenic units 193,197
helicenes 24,25,193
helicity descriptor 194
helicity symbols 193
(hemi)acetals 163
(hemi)ketals 163
hemialdehydes 115
hemiamides 115
heteranes 146, 148
hetero atoms at fusion positions 51,61
hetero bridges 65
heterocyclic systems 43
-, acylated 135
-, bridged 65-67
-, cationic 63, 103
-, exceptional names for benzo bicycles
60
-, fused 57 - 64
-, fused spirocyclic 64
-, Hantzsch-Widman names 54-57
-,linked 64
-, peripheral (final) numbering 61
-, priorities (seniorities) 57 - 60
-, replacement names 51- 54,64,67
-, trivial names 43-51
heteromonocyclic systems 53
higher membered rings 22
higher order components 21, 26
history of organic chemical nomenclature 4
homo 87,89,204
hydrazides 142
hydrazines 141
