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Fulvenes are the class of hydrocarbon obtained by formally cross-conjugating one ring and methylidene through a common exocyclic double bond.^[1]^[2]

The name is derived from the fulvene. which has one pentagonal ring. Pentafulvene is also called simply fulvene, the parent structure of this class.

Fulvenes are isomer of annulene.

^ Agranat, Israel (2012), "Ground-State Versus Excited-State Polarity of Triafulvenes: A Study of Solvent Effects on Molecular Electronic Spectra", The Jerusalem Symposia on Quantum Chemistry and Biochemistry, 8: 573–583, doi:10.1007/978-94-010-1837-1_36
^ Neuenschwander, Markus (1986), "Synthetic and NMR spectroscopic investigations of fulvenes and fulvalenes" (PDF), Pure&AppI. Chem., 58 (1): 55–66

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