Beilstein Journal of Organic Chemistry (Oct 2015)

Asymmetric 1,4-bis(ethynyl)bicyclo[2.2.2]octane rotators via monocarbinol functionalization. Ready access to polyrotors

  • Cyprien Lemouchi,
  • Patrick Batail

DOI
https://doi.org/10.3762/bjoc.11.202
Journal volume & issue
Vol. 11, no. 1
pp. 1881 – 1885

Abstract

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Asymmetric rotators with a 1,4-bis(ethynyl)bicyclo[2.2.2]octane (BCO) core are needed for engineering crystalline arrays of functional molecular rotors. Their synthesis uses carbinol, 2-methyl-3-butyn-2-ol, as a protecting group because of its polar character and its ability to sustain orthogonal functionalization with the further advantage of being readily removed. The synthesis in good yields of unprecedented asymmetric rotors and polyrotors demonstrates the efficiency of this strategy.

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