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, M.L., D'Accorso, N.B., Pellón, R.F., Docampo, M.L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00397911_v37_n23_p4209_Fascio
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spelling todo:paper_00397911_v37_n23_p4209_Fascio2023-10-03T14:49:57Z Synthesis of novel carbohydrate acridinone derivatives with potential biological activities using 1,3-dipolar cycloaddition Fascio, M.L. D'Accorso, N.B. Pellón, R.F. Docampo, M.L. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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, M.L.
D'Accorso, N.B.
Pellón, R.F.
Docampo, M.L.
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.
format JOUR
author Fascio, M.L.
D'Accorso, N.B.
Pellón, R.F.
Docampo, M.L.
author_facet Fascio, M.L.
D'Accorso, N.B.
Pellón, R.F.
Docampo, M.L.
author_sort Fascio, M.L.
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
url http://hdl.handle.net/20.500.12110/paper_00397911_v37_n23_p4209_Fascio
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AT pellonrf synthesisofnovelcarbohydrateacridinonederivativeswithpotentialbiologicalactivitiesusing13dipolarcycloaddition
AT docampoml synthesisofnovelcarbohydrateacridinonederivativeswithpotentialbiologicalactivitiesusing13dipolarcycloaddition
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