Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition

Novel 10-{[3-(6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)- 4,5-dihydro-5-isoxazolyl]methyl}-9(10H)-acridinone derivatives (13-16) were synthesized by 1,3-dipolar cycloaddition using the carbohydrate derivative as dipole and different 10-allyl-9(10H)-acridinone derivatives (9-12) as...

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Autores principales: Fascio, Mirta Liliana, D'Accorso, Norma Beatriz
Publicado: 2007
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v37_n23_p4209_Fascio
http://hdl.handle.net/20.500.12110/paper_00397911_v37_n23_p4209_Fascio
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spelling paper:paper_00397911_v37_n23_p4209_Fascio2023-06-08T15:03:41Z Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition Fascio, Mirta Liliana D'Accorso, Norma Beatriz 1,3-dipolar cycloaddition Acridinones Carbohydrates Isoxazolines N-allylation 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 4 methoxy 9(10h) acridinone 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone 10 allyl 3 chloro 5 methoxy 9(10h) acridinone 10 allyl 3 chloro 9(10h) acridinone 10 allyl 4 methoxy 9(10h) acridinone 10 allyl 9(10h) acridinone 3 chloro 10 [[3 ( hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 6 methoxy 9(10h) acridinone 3 chloro 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone acridinone derivative carbohydrate derivative organic compound unclassified drug article cycloaddition drug activity drug determination drug structure drug synthesis spectroscopy structure analysis Novel 10-{[3-(6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)- 4,5-dihydro-5-isoxazolyl]methyl}-9(10H)-acridinone derivatives (13-16) were synthesized by 1,3-dipolar cycloaddition using the carbohydrate derivative as dipole and different 10-allyl-9(10H)-acridinone derivatives (9-12) as dipolarophiles. The new cycloadducts as well as the dipolarophiles precursors were characterized spectroscopically. Copyright © Taylor & Francis Group, LLC. Fil:Fascio, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2007 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v37_n23_p4209_Fascio http://hdl.handle.net/20.500.12110/paper_00397911_v37_n23_p4209_Fascio
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 1,3-dipolar cycloaddition
Acridinones
Carbohydrates
Isoxazolines
N-allylation
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 4 methoxy 9(10h) acridinone
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
10 allyl 3 chloro 5 methoxy 9(10h) acridinone
10 allyl 3 chloro 9(10h) acridinone
10 allyl 4 methoxy 9(10h) acridinone
10 allyl 9(10h) acridinone
3 chloro 10 [[3 ( hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 6 methoxy 9(10h) acridinone
3 chloro 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
acridinone derivative
carbohydrate derivative
organic compound
unclassified drug
article
cycloaddition
drug activity
drug determination
drug structure
drug synthesis
spectroscopy
structure analysis
spellingShingle 1,3-dipolar cycloaddition
Acridinones
Carbohydrates
Isoxazolines
N-allylation
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 4 methoxy 9(10h) acridinone
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
10 allyl 3 chloro 5 methoxy 9(10h) acridinone
10 allyl 3 chloro 9(10h) acridinone
10 allyl 4 methoxy 9(10h) acridinone
10 allyl 9(10h) acridinone
3 chloro 10 [[3 ( hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 6 methoxy 9(10h) acridinone
3 chloro 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
acridinone derivative
carbohydrate derivative
organic compound
unclassified drug
article
cycloaddition
drug activity
drug determination
drug structure
drug synthesis
spectroscopy
structure analysis
Fascio, Mirta Liliana
D'Accorso, Norma Beatriz
Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
topic_facet 1,3-dipolar cycloaddition
Acridinones
Carbohydrates
Isoxazolines
N-allylation
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 4 methoxy 9(10h) acridinone
10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
10 allyl 3 chloro 5 methoxy 9(10h) acridinone
10 allyl 3 chloro 9(10h) acridinone
10 allyl 4 methoxy 9(10h) acridinone
10 allyl 9(10h) acridinone
3 chloro 10 [[3 ( hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 6 methoxy 9(10h) acridinone
3 chloro 10 [[3 (6 hydroxy 2,2 dimethyltetrahydrofuro[2,3 d][1,3]dioxol 5 yl) 4,5 dihydro 5 isoxazolyl]methyl] 9(10h) acridinone
acridinone derivative
carbohydrate derivative
organic compound
unclassified drug
article
cycloaddition
drug activity
drug determination
drug structure
drug synthesis
spectroscopy
structure analysis
description Novel 10-{[3-(6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)- 4,5-dihydro-5-isoxazolyl]methyl}-9(10H)-acridinone derivatives (13-16) were synthesized by 1,3-dipolar cycloaddition using the carbohydrate derivative as dipole and different 10-allyl-9(10H)-acridinone derivatives (9-12) as dipolarophiles. The new cycloadducts as well as the dipolarophiles precursors were characterized spectroscopically. Copyright © Taylor & Francis Group, LLC.
author Fascio, Mirta Liliana
D'Accorso, Norma Beatriz
author_facet Fascio, Mirta Liliana
D'Accorso, Norma Beatriz
author_sort Fascio, Mirta Liliana
title Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
title_short Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
title_full Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
title_fullStr Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
title_full_unstemmed Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
title_sort synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition
publishDate 2007
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v37_n23_p4209_Fascio
http://hdl.handle.net/20.500.12110/paper_00397911_v37_n23_p4209_Fascio
work_keys_str_mv AT fasciomirtaliliana synthesisofnovelcarbohydrateacridinonederivativeswithpotentialbiologicalactivitiesusing13dipolarcycloaddition
AT daccorsonormabeatriz synthesisofnovelcarbohydrateacridinonederivativeswithpotentialbiologicalactivitiesusing13dipolarcycloaddition
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