Photoinduced 1,2,3,4-tetrahydropyridine ring conversions

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Standard

Photoinduced 1,2,3,4-tetrahydropyridine ring conversions. / Turovska, Baiba; Lund, Henning; Lusis, Viesturs; Lielpetere, Anna; Liepins, Edvards; Beljakovs, Sergejs; Goba, Inguna; Stradins, Janis.

I: Beilstein Journal of Organic Chemistry, Bind 11, 2015, s. 2166-2170.

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Harvard

Turovska, B, Lund, H, Lusis, V, Lielpetere, A, Liepins, E, Beljakovs, S, Goba, I & Stradins, J 2015, 'Photoinduced 1,2,3,4-tetrahydropyridine ring conversions', Beilstein Journal of Organic Chemistry, bind 11, s. 2166-2170. https://doi.org/10.3762/bjoc.11.234

APA

Turovska, B., Lund, H., Lusis, V., Lielpetere, A., Liepins, E., Beljakovs, S., Goba, I., & Stradins, J. (2015). Photoinduced 1,2,3,4-tetrahydropyridine ring conversions. Beilstein Journal of Organic Chemistry, 11, 2166-2170. https://doi.org/10.3762/bjoc.11.234

CBE

Turovska B, Lund H, Lusis V, Lielpetere A, Liepins E, Beljakovs S, Goba I, Stradins J. 2015. Photoinduced 1,2,3,4-tetrahydropyridine ring conversions. Beilstein Journal of Organic Chemistry. 11:2166-2170. https://doi.org/10.3762/bjoc.11.234

MLA

Turovska, Baiba o.a.. "Photoinduced 1,2,3,4-tetrahydropyridine ring conversions". Beilstein Journal of Organic Chemistry. 2015, 11. 2166-2170. https://doi.org/10.3762/bjoc.11.234

Vancouver

Turovska B, Lund H, Lusis V, Lielpetere A, Liepins E, Beljakovs S o.a. Photoinduced 1,2,3,4-tetrahydropyridine ring conversions. Beilstein Journal of Organic Chemistry. 2015;11:2166-2170. https://doi.org/10.3762/bjoc.11.234

Author

Turovska, Baiba ; Lund, Henning ; Lusis, Viesturs ; Lielpetere, Anna ; Liepins, Edvards ; Beljakovs, Sergejs ; Goba, Inguna ; Stradins, Janis. / Photoinduced 1,2,3,4-tetrahydropyridine ring conversions. I: Beilstein Journal of Organic Chemistry. 2015 ; Bind 11. s. 2166-2170.

Bibtex

@article{f7d289d0dc464c7b8c66e12e4d476895,
title = "Photoinduced 1,2,3,4-tetrahydropyridine ring conversions",
abstract = "Stable heterocyclic hydroperoxide can be easily prepared as a product of fast oxidation of a 1,2,3,4-tetrahydropyridine by O-3(2) if the solution is exposed to sunlight. The driving force for the photoinduced electron transfer is calculated from electrochemical and spectroscopic data. The outcome of the reaction depends on the light intensity and the concentration of O-2. In the solid state the heterocyclic hydroperoxide is stable; in solution it is involved in further reactions.",
keywords = "heterocyclic hydroperoxide, oxaziridine, photoinduced electron transfer, pyrrolidine, tetrahydropyridine, SUPEROXIDE ANION, HANTZSCH 1,4-DIHYDROPYRIDINES, OXIDATION, REDUCTION, OXYGEN, DIOXYGEN, KINETICS, ELECTRON, ANALOGS, COUPLE",
author = "Baiba Turovska and Henning Lund and Viesturs Lusis and Anna Lielpetere and Edvards Liepins and Sergejs Beljakovs and Inguna Goba and Janis Stradins",
year = "2015",
doi = "10.3762/bjoc.11.234",
language = "English",
volume = "11",
pages = "2166--2170",
journal = "Beilstein Journal of Organic Chemistry",
issn = "2195-951X",
publisher = "Beilstein - Institut zur Foerderung der Chemischen Wissenschaften",

}

RIS

TY - JOUR

T1 - Photoinduced 1,2,3,4-tetrahydropyridine ring conversions

AU - Turovska, Baiba

AU - Lund, Henning

AU - Lusis, Viesturs

AU - Lielpetere, Anna

AU - Liepins, Edvards

AU - Beljakovs, Sergejs

AU - Goba, Inguna

AU - Stradins, Janis

PY - 2015

Y1 - 2015

N2 - Stable heterocyclic hydroperoxide can be easily prepared as a product of fast oxidation of a 1,2,3,4-tetrahydropyridine by O-3(2) if the solution is exposed to sunlight. The driving force for the photoinduced electron transfer is calculated from electrochemical and spectroscopic data. The outcome of the reaction depends on the light intensity and the concentration of O-2. In the solid state the heterocyclic hydroperoxide is stable; in solution it is involved in further reactions.

AB - Stable heterocyclic hydroperoxide can be easily prepared as a product of fast oxidation of a 1,2,3,4-tetrahydropyridine by O-3(2) if the solution is exposed to sunlight. The driving force for the photoinduced electron transfer is calculated from electrochemical and spectroscopic data. The outcome of the reaction depends on the light intensity and the concentration of O-2. In the solid state the heterocyclic hydroperoxide is stable; in solution it is involved in further reactions.

KW - heterocyclic hydroperoxide

KW - oxaziridine

KW - photoinduced electron transfer

KW - pyrrolidine

KW - tetrahydropyridine

KW - SUPEROXIDE ANION

KW - HANTZSCH 1,4-DIHYDROPYRIDINES

KW - OXIDATION

KW - REDUCTION

KW - OXYGEN

KW - DIOXYGEN

KW - KINETICS

KW - ELECTRON

KW - ANALOGS

KW - COUPLE

U2 - 10.3762/bjoc.11.234

DO - 10.3762/bjoc.11.234

M3 - Journal article

C2 - 26664638

VL - 11

SP - 2166

EP - 2170

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

SN - 2195-951X

ER -