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

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Standard

Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects. / Angelis, Yiannis S.; Hatzakis, Nikos S.; Smonou, Ioulia; Orfanopoulos, Michael.

I: Tetrahedron Letters, Bind 42, Nr. 22, 2001, s. 3753-3756.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Angelis, YS, Hatzakis, NS, Smonou, I & Orfanopoulos, M 2001, 'Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects', Tetrahedron Letters, bind 42, nr. 22, s. 3753-3756. https://doi.org/10.1016/S0040-4039(01)00539-1

APA

Angelis, Y. S., Hatzakis, N. S., Smonou, I., & Orfanopoulos, M. (2001). Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects. Tetrahedron Letters, 42(22), 3753-3756. https://doi.org/10.1016/S0040-4039(01)00539-1

Vancouver

Angelis YS, Hatzakis NS, Smonou I, Orfanopoulos M. Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects. Tetrahedron Letters. 2001;42(22):3753-3756. https://doi.org/10.1016/S0040-4039(01)00539-1

Author

Angelis, Yiannis S. ; Hatzakis, Nikos S. ; Smonou, Ioulia ; Orfanopoulos, Michael. / Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects. I: Tetrahedron Letters. 2001 ; Bind 42, Nr. 22. s. 3753-3756.

Bibtex

@article{75796ebf67a34f1dad552708585a9a03,
title = "Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects",
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.",
keywords = "Dioxiranes, Isotope effects, Mechanisms",
author = "Angelis, {Yiannis S.} and Hatzakis, {Nikos S.} and Ioulia Smonou and Michael Orfanopoulos",
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.",
year = "2001",
doi = "10.1016/S0040-4039(01)00539-1",
language = "English",
volume = "42",
pages = "3753--3756",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Pergamon Press",
number = "22",

}

RIS

TY - JOUR

T1 - Oxidation of benzyl alcohols by dimethyldioxirane. The question of concerted versus stepwise mechanisms probed by kinetic isotope effects

AU - Angelis, Yiannis S.

AU - Hatzakis, Nikos S.

AU - Smonou, Ioulia

AU - Orfanopoulos, Michael

N1 - 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.

PY - 2001

Y1 - 2001

N2 - 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.

AB - 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.

KW - Dioxiranes

KW - Isotope effects

KW - Mechanisms

U2 - 10.1016/S0040-4039(01)00539-1

DO - 10.1016/S0040-4039(01)00539-1

M3 - Journal article

AN - SCOPUS:0035962969

VL - 42

SP - 3753

EP - 3756

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 22

ER -

ID: 286412620