(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one
<i>(E)</i>-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one was synthesized via the oxidative ring opening reaction of 2-(5-methylfuran-2-yl)-1-phenylethanone oxime, followed by the iodine mediated isomerization.
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MDPI AG
2019-09-01
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Online Access: | https://www.mdpi.com/1422-8599/2019/3/M1081 |
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doaj-7d7856971b2b45eb94339488339346292020-11-24T22:14:36ZengMDPI AGMolbank1422-85992019-09-0120193M108110.3390/M1081M1081(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-oneNattawut Sawengngen0Alexandra A. Kolodina1Olga V. Serdyuk2Department of Chemistry and Pharmacy, Institute of Organic Chemistry I, University of Erlangen-Nuremberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, GermanyInstitute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki St., Rostov on Don 344090, RussiaDepartment of Chemistry and Pharmacy, Institute of Organic Chemistry I, University of Erlangen-Nuremberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, Germany<i>(E)</i>-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one was synthesized via the oxidative ring opening reaction of 2-(5-methylfuran-2-yl)-1-phenylethanone oxime, followed by the iodine mediated isomerization.https://www.mdpi.com/1422-8599/2019/3/M1081oxazolefuranRORC reaction(<i>E,Z</i>)-isomerization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nattawut Sawengngen Alexandra A. Kolodina Olga V. Serdyuk |
spellingShingle |
Nattawut Sawengngen Alexandra A. Kolodina Olga V. Serdyuk (<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one Molbank oxazole furan RORC reaction (<i>E,Z</i>)-isomerization |
author_facet |
Nattawut Sawengngen Alexandra A. Kolodina Olga V. Serdyuk |
author_sort |
Nattawut Sawengngen |
title |
(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one |
title_short |
(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one |
title_full |
(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one |
title_fullStr |
(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one |
title_full_unstemmed |
(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one |
title_sort |
(<i>e</i>)-4-(3-phenylisoxazol-5-yl)but-3-en-2-one |
publisher |
MDPI AG |
series |
Molbank |
issn |
1422-8599 |
publishDate |
2019-09-01 |
description |
<i>(E)</i>-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one was synthesized via the oxidative ring opening reaction of 2-(5-methylfuran-2-yl)-1-phenylethanone oxime, followed by the iodine mediated isomerization. |
topic |
oxazole furan RORC reaction (<i>E,Z</i>)-isomerization |
url |
https://www.mdpi.com/1422-8599/2019/3/M1081 |
work_keys_str_mv |
AT nattawutsawengngen iei43phenylisoxazol5ylbut3en2one AT alexandraakolodina iei43phenylisoxazol5ylbut3en2one AT olgavserdyuk iei43phenylisoxazol5ylbut3en2one |
_version_ |
1725798051252011008 |