Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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.
Originalsprog | Engelsk |
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Tidsskrift | Tetrahedron Letters |
Vol/bind | 42 |
Udgave nummer | 22 |
Sider (fra-til) | 3753-3756 |
Antal sider | 4 |
ISSN | 0040-4039 |
DOI | |
Status | Udgivet - 2001 |
Eksternt udgivet | Ja |
ID: 286412620