DOI: 10.1351/goldbook
CH4N41 molecule
C2H2N2O2 molecules
C2H3N32 molecules
C2H3N31 molecule
C2H4N2O2 molecules
C2H4NS21 molecule
C2H4O4 molecules
C2H4O31 molecule
C2H4S1 molecule
C2H5N1 molecule
C2H6N41 molecule
C3H3NO1 molecule
C3H4FeN21 molecule
C3H4N22 molecules
C3H4O21 molecule
C3H4OS1 molecule
C3H6FeN21 molecule
C3H5NO3 molecules
C3H5NO1 molecule
C3H6N21 molecule
C3H5NS1 molecule
C3H6Ni1 molecule
C3H6O2 molecules
C3H6O22 molecules
C3H6OS1 molecule
C3H7N6 molecules
C3H7NO1 molecule
C3H7NS1 molecule
C3H7NS2 molecules
C4H41 molecule
C4H4N24 molecules
C4H4N22 molecules
C4H4O1 molecule
C4H4O21 molecule
C4H4S1 molecule
C4H4S21 molecule
C4H10N21 molecule
C4H5N4 molecules
C4H5N1 molecule
C4H6N21 molecule
C4H6N22 molecules
C4H6O2 molecules
C4H6O1 molecule
C4H6S1 molecule
C4H7N2 molecules
C4H7N1 molecule
C4H7NS1 molecule
C4H89 molecules
C4H8N21 molecule
C4H8O15 molecules
C4H8O22 molecules
C4H8S1 molecule
C4H9N7 molecules
C4H9NS1 molecule
C5H5N11 molecules
C5H5N1 molecule
C5H5P1 molecule
C5H67 molecules
C5H6O3 molecules
C5H6O1 molecule
C5H7N3 molecules
C5H7N1 molecule
C5H7P1 molecule
C5H85 molecules
C5H8O5 molecules
C5H8O2 molecules
C5H1022 molecules
C5H10O17 molecules
C5H11N1 molecule
C6H41 molecule
C6H6138 molecules
C6H6O1 molecule
C6H810 molecules
C6H816 molecules
C6H1012 molecules
C6H1229 molecules
C6H13N1 molecule
C7H143 molecules
C7H88 molecules
C8H141 molecule
C8H162 molecules
C11H14N41 molecule
C12H161 molecule
C12H16N41 molecule
C12H181 molecule
C12H24O64 molecules
C12H26N2O41 molecule
C18H38N23 molecules
H6O3Si31 molecule
1 molecule
verdazyl radicals
2 molecules
sydnone imines
sydnones
tele-substitution
osotriazoles
Herz compounds
4 molecules
arene epoxides
epihalohydrins
epoxy compounds
valence tautomerization
molozonides
ozonides
episulfonium ions
aza-di-π-methane rearrangement
munchnones
hemes (heme derivatives)
pros
purine bases
lignans
sulfonphthaleins
3 molecules
azlactones
carboxamidines
penems
metallacycloalkanes
dyotropic rearrangement
Paterno–Büchi reaction
acetonides
cyclic acid anhydrides (cyclic anhydrides)
6 molecules
cephalosporins
cephams
lactams
penams
penicillins
imides
ring assembly
pyrimidine bases
topomerization
folates
heteroarenes
heteroarynes
furocoumarins
isolated double bonds
barbiturates
dipyrrins
porphyrins
tetrapyrroles
indicated hydrogen
xanthene dyes
cheletropic reaction
corrinoids (cobalamines, corphyrins, corrins, vitamin B12 compounds)
heteroaryl groups
9 molecules
nonclassical structure
de Mayo reaction
cis-trans isomers
cycloalkanes
extrusion transformation
oxocarbons
polyhedranes
flavins
15 molecules
aldoses
fulgides
furanoses
Haworth representation
nucleotides
phthaleins
ribonucleotides
rotenoids
tautomerism
lactides
sulfonium compounds
7 molecules
heterocyclyl groups
imidines
imino acids
pseudo-asymmetric carbon atom
11 molecules
anhydro bases
cyanine dyes
Dimroth–Reichardt ET parameter
nucleophilic catalysis
pseudo bases
viologens
bicycle rearrangement
alternant
fulvalenes
fulvenes
quinarenes
spiro compounds
rhodamine dyes
Reissert compounds
5 molecules
Bredt's rule
cycloaddition
polyquinanes (polyquinenes)
enoses
flavonoids (isoflavonoids and neoflavonoids)
isocoumarins
coumarins
22 molecules
α (alpha), β (beta)
abeo-
cyclo-
endo, exo, syn, anti
envelope conformation
iridoids
meso-compound
monosaccharides
prostaglandins
seco-
steroids
17 molecules
amino sugars
anomeric effect
glycolipids
glycosides
ketoses
sulfatides
uronic acids
aryne
138 molecules
chain transfer
cine-substitution
common-ion effect (on rates)
cyanides
cyclophanes
dehydroarenes
depsides
diazooxides
electrophile (electrophilic)
fragmentation
helicenes
helicity
hyperconjugation
isodesmic reaction
isotope exchange
isotopic scrambling
Kekulé structure (for aromatic compounds)
leaving group
molecular rearrangement
NIH shift
nitrilium ions
ortho- and peri-fused (polycyclic compounds)
ortho-fused (polycyclic compounds)
π-adduct
phenols
photo-Fries rearrangement
planar chirality
polyketides
quinhydrones
tetracyclines
non-Kekulé molecules
acenes
acid anhydrides
acylals
acyl groups
amides
amidium ions
aminium ions
ammoniumyl radical ions
anilides
anthocyanidins
anti
aryl cations
arylene groups
aryl groups
axial chirality
azoxy compounds
benzylic groups
benzylic intermediates
betaines
biradical
bisphenols
catalytic dehydrocyclization
catalytic hydrogenolysis
catecholamines
chain reaction
10 molecules
quinomethanes
quinones
16 molecules
electrocyclic reaction
quinonimines (quinone imines)
tropilidenes [obsolete]
12 molecules
attachment
carotenoids
half-chair
retinoids
retro
29 molecules
acyl halides
axial (equatorial)
carbenes
chair, boat, twist
glycosylamines
propellanes
8 molecules
annulenylidenes
tropolones
tropones
crown conformation
tub conformation
crown
in-out isomerism
cryptand
cyclosiloxanes