4.8 Review

Regioselectivity in the ring opening of non-activated aziridines

Journal

CHEMICAL SOCIETY REVIEWS
Volume 41, Issue 2, Pages 643-665

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cs15140a

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Funding

  1. Research Foundation-Flanders (Belgium) (FWO-Vlaanderen)
  2. Ghent University (GOA)
  3. National Research Foundation (NRF) [2011-0012379]
  4. Center for Bioactive Molecular Hybrides

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In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate aziridinium salts will be dealt with. Emphasis will be put on the relationship between the observed regioselectivity and inherent structural features such as the nature of the C2 aziridine substituent and the nature of the electrophile and the nucleophile. This overview should allow chemists to gain insight into the factors governing the regioselectivity in aziridinium ring openings (81 references).

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