Propargyl

In organic chemistry, propargyl is an alkyl functional group of 2-propynyl with the structure HC≡C−CH2−, derived from the alkyne propyne.

Chemical structure of the propargyl group.

The term propargylic refers to a saturated position (sp3-hybridized) on a molecular framework next to an alkynyl group. The name comes from mix of propene and argentum, which refers to the typical reaction of the terminal alkynes with silver salts.

The term homopropargylic designates in the same manner

  • a saturated position on a molecular framework next to a propargylic group and thus two bonds from an alkyne moiety.[1]
  • a 3-butynyl fragment, HCC-CH2CH2-, or substituted homologue.

See also

References
  1. Ferreira, Franck; Denichoux, Aurélien; Chemla, Fabrice; Bejjani, Joseph (2004). "Highly Diastereoselective Syntheses of Propargylic Acid and Homopropargylic Systems". Synlett (12): 2051–2065. doi:10.1055/s-2004-832816.
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