(<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.

Bibliographic Details
Main Authors: Nattawut Sawengngen, Alexandra A. Kolodina, Olga V. Serdyuk
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2019/3/M1081
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spelling 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
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