Photoinduced 1,2,3,4-Tetrahydropyridine Ring Conversions
Beilstein Journal of Organic Chemistry
2015
Baiba Turovska,
H. Lund,
Viesturs Lūsis,
A. Lielpetere,
Edvards Liepiņš,
Sergejs Beļakovs,
I. Goba,
J. Stradiņš
Stable heterocyclic hydroperoxide can be easily prepared as a product of fast oxidation of a 1,2,3,4-tetrahydropyridine by 3O2 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 O2. In the solid state the heterocyclic hydroperoxide is stable; in solution it is involved in further reactions.
Atslēgas vārdi
heterocyclic hydroperoxide; oxaziridine; photoinduced electron transfer; pyrrolidine; tetrahydropyridine
DOI
10.3762/bjoc.11.234
Hipersaite
http://www.beilstein-journals.org/bjoc/single/articleFullText.htm?publicId=1860-5397-11-234
Turovska, B., Lund, H., Lūsis, V., Lielpetere, A., Liepiņš, E., Beļakovs, S., Goba, I., Stradiņš, J. Photoinduced 1,2,3,4-Tetrahydropyridine Ring Conversions. Beilstein Journal of Organic Chemistry, 2015, No. 11, 2166.-2170.lpp. ISSN 1860-5397. Pieejams: doi:10.3762/bjoc.11.234
Publikācijas valoda
English (en)