Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones

A facile photochemical preparation of 5-, 6-, and 7-substituted chroman-4-ones from aryl 3-methyl-2-butenoate esters is described. The two-phase base-catalyzed method relies upon two consecutive processes in one-pot reaction through a photo-Fries rearrangement and a based-catalyzed intramolecular ox...

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Autores principales: Iguchi, D., Erra-Balsells, R., Bonesi, S.M.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00404039_v55_n33_p4653_Iguchi
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spelling todo:paper_00404039_v55_n33_p4653_Iguchi2023-10-03T14:50:57Z Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones Iguchi, D. Erra-Balsells, R. Bonesi, S.M. Aryl esters Chroman-4-ones oxa-Michael addition photo-Fries rearrangement Two-phase reaction 3 methyl 2 butenoate ester derivative 4 chromanone derivative cyclohexane ester derivative natural product unclassified drug Article catalysis cyclization Michael addition photochemistry quantum yield reaction analysis A facile photochemical preparation of 5-, 6-, and 7-substituted chroman-4-ones from aryl 3-methyl-2-butenoate esters is described. The two-phase base-catalyzed method relies upon two consecutive processes in one-pot reaction through a photo-Fries rearrangement and a based-catalyzed intramolecular oxa-Michael addition to afford the desired products. © 2014 Elsevier Ltd. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00404039_v55_n33_p4653_Iguchi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Aryl esters
Chroman-4-ones
oxa-Michael addition
photo-Fries rearrangement
Two-phase reaction
3 methyl 2 butenoate ester derivative
4 chromanone derivative
cyclohexane
ester derivative
natural product
unclassified drug
Article
catalysis
cyclization
Michael addition
photochemistry
quantum yield
reaction analysis
spellingShingle Aryl esters
Chroman-4-ones
oxa-Michael addition
photo-Fries rearrangement
Two-phase reaction
3 methyl 2 butenoate ester derivative
4 chromanone derivative
cyclohexane
ester derivative
natural product
unclassified drug
Article
catalysis
cyclization
Michael addition
photochemistry
quantum yield
reaction analysis
Iguchi, D.
Erra-Balsells, R.
Bonesi, S.M.
Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
topic_facet Aryl esters
Chroman-4-ones
oxa-Michael addition
photo-Fries rearrangement
Two-phase reaction
3 methyl 2 butenoate ester derivative
4 chromanone derivative
cyclohexane
ester derivative
natural product
unclassified drug
Article
catalysis
cyclization
Michael addition
photochemistry
quantum yield
reaction analysis
description A facile photochemical preparation of 5-, 6-, and 7-substituted chroman-4-ones from aryl 3-methyl-2-butenoate esters is described. The two-phase base-catalyzed method relies upon two consecutive processes in one-pot reaction through a photo-Fries rearrangement and a based-catalyzed intramolecular oxa-Michael addition to afford the desired products. © 2014 Elsevier Ltd.
format JOUR
author Iguchi, D.
Erra-Balsells, R.
Bonesi, S.M.
author_facet Iguchi, D.
Erra-Balsells, R.
Bonesi, S.M.
author_sort Iguchi, D.
title Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
title_short Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
title_full Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
title_fullStr Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
title_full_unstemmed Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
title_sort expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
url http://hdl.handle.net/20.500.12110/paper_00404039_v55_n33_p4653_Iguchi
work_keys_str_mv AT iguchid expeditiousphotochemicalreactiontowardthepreparationofsubstitutedchroman4ones
AT errabalsellsr expeditiousphotochemicalreactiontowardthepreparationofsubstitutedchroman4ones
AT bonesism expeditiousphotochemicalreactiontowardthepreparationofsubstitutedchroman4ones
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