4.8 Article

Extension of the Bambus[n]uril Family: Microwave Synthesis and Reactivity of Allylbambus[n]urils

Journal

ORGANIC LETTERS
Volume 15, Issue 3, Pages 480-483

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol303277u

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Funding

  1. French Ministry of Research [ANR-09-BLAN-0182-01]
  2. Agence Nationale de la Recherche (ANR) [ANR-09-BLAN-0182] Funding Source: Agence Nationale de la Recherche (ANR)

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Microwave irradiations allow the preparation of unsaturated bambusurils in 85% yield compared to 20% yield under classical reaction conditions. Five new bambusurils were synthesized including unsaturated derivatives Allyl(8)BU[4] and Allyl(12)BU[6] bearing diallylglycoluril units. The reactivity of Allyl(8)BU[4] was tested in a variety of organic reactions showing that this macrocycle acts as a classical double bond-bearing product. The first monofunctionalized bambusuril Allyl(7)HepBU[4] prepared by a cross metathesis reaction is also reported.

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