- chemrev.6b00210. PMID 28151643. Bergmann, E. D. (1968). "
Fulvenes and
Substituted Fulvenes".
Chemical Reviews. 68: 41–84. doi:10.1021/cr60251a002. Kaplan...
-
derived from
fulvene,
which has one
pentagonal ring.
Other examples include methylenecyclopropene (triafulvene) and heptafulvene.
Fulvenes are generally...
-
exocyclic double bond attached.
Methylenecyclopropene is the
smallest of the
fulvenes (a
family of unstable,
cyclic molecules,
conjugated transversally with...
- ([22]-annulene)
Wikimedia Commons has
media related to Annulenes.
Annulyne Circulene Fulvenes IUPAC,
Compendium of
Chemical Terminology, 2nd ed. (the "Gold Book") (1997)...
- exo products. (2)
Fulvenes react similarly,
although selective [6+4]
reactions require the use of an electron-rich diene.
Fulvene's frontier orbitals...
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Benzene Benzvalene Bicyclopropenyl 1,2,3-Cyclohexatriene
Dewar benzene Fulvene Prismane [3]Radialene 3-Methylidenepent-1-en-4-yne
Hexadiyne 1,3-Hexadiyne...
- Neuenschwander,
Markus (1986), "Synthetic and NMR
spectroscopic investigations of
fulvenes and fulvalenes" (PDF), Pure Appl. Chem., 58 (1): 55–66, doi:10.1351/pac198658010055...
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Perchlorofulvalene (C4Cl4C)2 is
quite stable in
contrast to
fulvalene itself.
Fulvenes, (CH=CH)2C=CH2 and
substituted derivatives Tetrathiafulvalene, C2H2S2C=CS2C2H2...
- the π-Electronic
Structure of Singlet, Triplet, and
Quintet States of
Fulvenes and
Fulvalenes Using the
Electron Localization Function". The
Journal of...
- η4- and η6-
fulvene complexes....