4.6 Review

Recent advances in fluoride-free aryne generation from arene precursors

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 43, Pages 9044-9056

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob01947e

Keywords

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Funding

  1. EPSRC [EP/M026221/1]
  2. QMUL
  3. Engineering and Physical Sciences Research Council [EP/M026221/1] Funding Source: researchfish
  4. EPSRC [EP/M026221/1] Funding Source: UKRI

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Aryne chemistry has experienced a remarkable renaissance in recent years, with a significant increase in the synthetic applications reported for these highly valuable reactive intermediates. This resurgence of interest is in part due to the introduction of ortho-silylaryl triflates as precursors which can be activated under mild conditions using fluoride. Alternative fluoride-free strategies have received interest in the last decade, with a number of precursors to arynes and their activators reported. These approaches offer alternative modes of reactivity which prove, in some cases, to be orthogonal to those of ortho-silylaryl triflates. This review highlights some of the more recent fluoride-free methodologies developed to access aryne intermediates that start from arene-based precursors.

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