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Abstract:

Irradiation of β-carboline derivatives gives two products involving the formation of new N-N or N-C bonds. On the basis of MS and 1H-NMR data dimeric structures were established. Some aspects of the photophysical process and of the radical nature of these dimerization reactions are discussed. © 1983.

Registro:

Documento: Artículo
Título:Photochemical dimerization of β-carboline alkaloids
Autor:Balsells, R.E.; Frasca, A.R.
Filiación:Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Pabellón 2, 3, Ciudad Universitaria, 1428-Buenos AiresArgentina
Palabras clave:beta carboline derivative; drug analysis; drug identification; drug structure; drug synthesis; harman derivative; harmine derivative; mass spectrometry; photochemistry; proton nuclear magnetic resonance; theoretical study
Año:1983
Volumen:39
Número:1
Página de inicio:33
Página de fin:39
DOI: http://dx.doi.org/10.1016/S0040-4020(01)97626-4
Título revista:Tetrahedron
Título revista abreviado:Tetrahedron
ISSN:00404020
CODEN:TETRA
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v39_n1_p33_Balsells

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Citas:

---------- APA ----------
Balsells, R.E. & Frasca, A.R. (1983) . Photochemical dimerization of β-carboline alkaloids. Tetrahedron, 39(1), 33-39.
http://dx.doi.org/10.1016/S0040-4020(01)97626-4
---------- CHICAGO ----------
Balsells, R.E., Frasca, A.R. "Photochemical dimerization of β-carboline alkaloids" . Tetrahedron 39, no. 1 (1983) : 33-39.
http://dx.doi.org/10.1016/S0040-4020(01)97626-4
---------- MLA ----------
Balsells, R.E., Frasca, A.R. "Photochemical dimerization of β-carboline alkaloids" . Tetrahedron, vol. 39, no. 1, 1983, pp. 33-39.
http://dx.doi.org/10.1016/S0040-4020(01)97626-4
---------- VANCOUVER ----------
Balsells, R.E., Frasca, A.R. Photochemical dimerization of β-carboline alkaloids. Tetrahedron. 1983;39(1):33-39.
http://dx.doi.org/10.1016/S0040-4020(01)97626-4