Abstract:
A convenient procedure for the synthesis of N-allyl substituted acridones under phase-transfer catalysis is reported using allyl bromide as alkylating agent. When propargyl bromide was used, in the same reaction conditions, no propynylacridone was detected in the reaction and only propadienylacridone was obtained in moderate yield.
Registro:
Documento: |
Artículo
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Título: | Synthesis of N-allyl and N-propadienylacridones using phase-transfer catalysis |
Autor: | Xuárez, L.; Pellón, R.F.; Fascio, M.; Montesano, V.; D'Accorso, N. |
Filiación: | Centro de Quimica Farmaceutica, Apartado 16042, La Habana, Cuba Departamento de Quimica Organica, Fac. de Ciencias Exactas y Naturales, Ciudad Universitaria, Buenos Aires, Argentina
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Palabras clave: | acridone derivative; alkylating agent; bromide; n allylacridone derivative; n propadienylacridone derivative; propadienylacridone; propargyl bromide; propynylacridone; unclassified drug; article; catalysis; chemical reaction; phase transition; reaction analysis; synthesis |
Año: | 2004
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Volumen: | 63
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Número: | 1
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Página de inicio: | 23
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Página de fin: | 28
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Título revista: | Heterocycles
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Título revista abreviado: | Heterocycles
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ISSN: | 03855414
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CODEN: | HTCYA
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CAS: | bromide, 24959-67-9
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Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03855414_v63_n1_p23_Xuarez |
Referencias:
- Abadi, A., Subbagh, E., Khamees, A., (1999) Arzneimittel-Forschun/Drug. Research, 49, p. 259
- Kawai, S., Tomono, Y., Katase, E., Ogawa, K., Yano, M., Takemura, Y., (1999) Leukemia Research, 23, p. 263
- Tabarrini, D., Cecchetti, V., Fravolini, A., Nocentini, G., Sabatini, S., (1999) J. Med. Chem., 42, p. 2136
- Fujioka, H., Kato, N., Fujika, M., Fujimura, K., Nishiyama, Y., (1990) Arzneimittel-Forschung/Drug. Research, 40, p. 1026
- Basco, L., Mitaku, S., Skaltsounis, A., Ravelomanantsoa, N., Le-Bras, J., (1994) Antimicrobial Agent and Chemotherapy, 38, p. 1169
- Takemura, Y., Ju-Ichi, M., Ito, C., Furukawa, H., Tokuda, H., (1995) Planta Med., 61, p. 366
- Turpin, J., Buckkeit, R., Derse, D., Hollingshead, M., (1998) Antimicrobial Agent and Chemotherapy, 2, p. 487
- Vance, J., Bastow, K., (1999) Biochemical Pharm., 58, p. 703
- Djeridi, D., Galy, J.P., Barbe, J., (1990) Heterocycles, 31, p. 1059
- Bemy, H., Bsiri, N., Clarbit, J., Galy, A., (1992) Arzneimittel-Forschung/Drug. Research, 42, p. 674
- Ngadi, L., Bsiri, N., Mahamoud, A., Galy, A., Galy, J.-P., (1993) Arzneimittel-Forschung/Drug. Research, 43, p. 480
- March, J., (1992) Advanced Organic Chemistry. Reactions, Mechanisms and Structure. Fourth Edition, p. 582. , by John Wiley and Sons Interscience Publications
Citas:
---------- APA ----------
Xuárez, L., Pellón, R.F., Fascio, M., Montesano, V. & D'Accorso, N.
(2004)
. Synthesis of N-allyl and N-propadienylacridones using phase-transfer catalysis. Heterocycles, 63(1), 23-28.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03855414_v63_n1_p23_Xuarez [ ]
---------- CHICAGO ----------
Xuárez, L., Pellón, R.F., Fascio, M., Montesano, V., D'Accorso, N.
"Synthesis of N-allyl and N-propadienylacridones using phase-transfer catalysis"
. Heterocycles 63, no. 1
(2004) : 23-28.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03855414_v63_n1_p23_Xuarez [ ]
---------- MLA ----------
Xuárez, L., Pellón, R.F., Fascio, M., Montesano, V., D'Accorso, N.
"Synthesis of N-allyl and N-propadienylacridones using phase-transfer catalysis"
. Heterocycles, vol. 63, no. 1, 2004, pp. 23-28.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03855414_v63_n1_p23_Xuarez [ ]
---------- VANCOUVER ----------
Xuárez, L., Pellón, R.F., Fascio, M., Montesano, V., D'Accorso, N. Synthesis of N-allyl and N-propadienylacridones using phase-transfer catalysis. Heterocycles. 2004;63(1):23-28.
Available from: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03855414_v63_n1_p23_Xuarez [ ]