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Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects

  • Yiannis S. Angelis
  • , Nikos S. Hatzakis
  • , Ioulia Smonou
  • , Michael Orfanopoulos*
  • *Corresponding author af dette arbejde

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Abstract

The primary and β-secondary kinetic isotope effects in the oxidation of secondary alcohols with dimethyl dioxirane were measured. The substantial primary and the absence of a β-secondary kinetic isotope effect support a concerted mechanism for the title reaction.

OriginalsprogEngelsk
TidsskriftTetrahedron Letters
Vol/bind42
Udgave nummer22
Sider (fra-til)3753-3756
Antal sider4
ISSN0040-4039
DOI
StatusUdgivet - 2001
Udgivet eksterntJa

Bibliografisk note

Funding Information:
We thank the Greek Secretariat of Research and Technology (ΠENEΔ 1999 to I.S. and ΠENEΔ 1999 to M.O.) for financial support and for a research fellowship to Y.S.A. and N.S.H. Professor W. Adam is also acknowledged for valuable comments.

Finansiering

We thank the Greek Secretariat of Research and Technology (ΠENEΔ 1999 to I.S. and ΠENEΔ 1999 to M.O.) for financial support and for a research fellowship to Y.S.A. and N.S.H. Professor W. Adam is also acknowledged for valuable comments.

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