4.8 Article

Triazene-Activated Donor-Acceptor Cyclopropanes: Ring-Opening and (3+2) Annulation Reactions

Journal

ORGANIC LETTERS
Volume 22, Issue 11, Pages 4517-4522

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c01527

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Funding

  1. Ecole Polytechnique Federale de Lausanne (EPFL)
  2. Swiss National Science Foundation [200021_165788]
  3. Swiss National Science Foundation (SNF) [200021_165788] Funding Source: Swiss National Science Foundation (SNF)

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Donor-acceptor cyclopropanes substituted with 3,3-dialkyltriazenyl groups are described herein. The strong electron-donating character of the triazene renders the cyclopropanes highly reactive, allowing for catalyst-free ring-opening reactions with methanol and tetracyanoethylene under mild conditions. The triazene-substituted cyclopropanes could also be used as substrates in Lewis acid catalyzed (3 + 2) annulations with silyl enol ethers.

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