4.7 Article

Cyclization and annulation reactions of nitrogen-substituted cyclopropanes and cyclobutanes

Journal

CHEMICAL COMMUNICATIONS
Volume 50, Issue 75, Pages 10912-10928

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc03194f

Keywords

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Funding

  1. Swiss National Science Foundation (SNSF) [200021_129874, 200020_149494]
  2. Swiss State Secretariat for Education, Research and Innovation [C10.0116, COST action CM0804]
  3. European Commission (Marie Curie IEF fellowship) [253274]
  4. F. Hoffmann-La Roche Ltd
  5. Swiss National Science Foundation (SNF) [200020_149494, 200021_129874] Funding Source: Swiss National Science Foundation (SNF)

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Cyclization and annulation reactions initiated by ring-opening of small rings, especially cyclopropanes and cyclobutanes are now well-established in synthetic chemistry. Nevertheless, the potential of aminocyclopropanes and cyclobutanes, an important subclass for the synthesis of nitrogen-rich building blocks, has remained unexploited for a long time, despite important pioneering results. In the last decade, the situation has changed dramatically and new catalytic methods have emerged both for cyclization and annulation reactions. The purpose of this feature article is to present recent progress in this area, including our own work using donor-acceptor cyclopropanes and cyclobutanes.

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