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

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

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
Eksternt udgivetJa

ID: 286412620