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Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones

A cascade reaction of 4-hydroxythiocoumarin and 4Н-chromene-3-carbaldehydes was developed, consisting of Knoevenagel condensation and oxa-6π electrocyclization in the presence of ammonium acetate as catalyst. A series of polycyclic acetals containing a fused thiocoumarin moiety were obtained

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Asıl Yazarlar: Demidov, O. P., Демидов, О. П.
Materyal Türü: Статья
Dil:English
Baskı/Yayın Bilgisi: Springer 2020
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Online Erişim:https://dspace.ncfu.ru/handle/20.500.12258/14619
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spelling ir-20.500.12258-146192020-11-13T12:12:38Z Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones Demidov, O. P. Демидов, О. П. 1H-benzo[f]chromene-2-carbaldehydes 4-hydroxythiocoumarin 4Н-chromene-3-carbaldehydes Electrocyclization Formal [3+3] cycloaddition Knoevenagel condensation A cascade reaction of 4-hydroxythiocoumarin and 4Н-chromene-3-carbaldehydes was developed, consisting of Knoevenagel condensation and oxa-6π electrocyclization in the presence of ammonium acetate as catalyst. A series of polycyclic acetals containing a fused thiocoumarin moiety were obtained 2020-11-10T12:20:22Z 2020-11-10T12:20:22Z 2020 Статья Semenova, I.A., Osipov, D.V., Popova, Y.V., Osyanin, V.A., Demidov, O.P., Klimochkin, Y.N. Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 9. - Pages 1218–1221 http://hdl.handle.net/20.500.12258/14619 en Chemistry of Heterocyclic Compounds application/pdf application/pdf Springer
institution СКФУ
collection Репозиторий
language English
topic 1H-benzo[f]chromene-2-carbaldehydes
4-hydroxythiocoumarin
4Н-chromene-3-carbaldehydes
Electrocyclization
Formal [3+3] cycloaddition
Knoevenagel condensation
spellingShingle 1H-benzo[f]chromene-2-carbaldehydes
4-hydroxythiocoumarin
4Н-chromene-3-carbaldehydes
Electrocyclization
Formal [3+3] cycloaddition
Knoevenagel condensation
Demidov, O. P.
Демидов, О. П.
Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
description A cascade reaction of 4-hydroxythiocoumarin and 4Н-chromene-3-carbaldehydes was developed, consisting of Knoevenagel condensation and oxa-6π electrocyclization in the presence of ammonium acetate as catalyst. A series of polycyclic acetals containing a fused thiocoumarin moiety were obtained
format Статья
author Demidov, O. P.
Демидов, О. П.
author_facet Demidov, O. P.
Демидов, О. П.
author_sort Demidov, O. P.
title Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
title_short Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
title_full Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
title_fullStr Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
title_full_unstemmed Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
title_sort formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4н-chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones
publisher Springer
publishDate 2020
url https://dspace.ncfu.ru/handle/20.500.12258/14619
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AT demidovop formal33cycloadditionreactionof4hydroxythiocoumarinto4nchromene3carbaldehydessynthesisofthiochromeno3456pyrano23bchromen6ones
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