(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one

Nattawut Sawengngen; Alexandra  A. Kolodina; Olga  V. Serdyuk

doi:10.3390/M1081

Molbank (Sep 2019)

(<i>E</i>)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one

Nattawut Sawengngen,
Alexandra A. Kolodina,
Olga V. Serdyuk

Affiliations

Nattawut Sawengngen: Department of Chemistry and Pharmacy, Institute of Organic Chemistry I, University of Erlangen-Nuremberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, Germany
Alexandra A. Kolodina: Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki St., Rostov on Don 344090, Russia
Olga V. Serdyuk: Department of Chemistry and Pharmacy, Institute of Organic Chemistry I, University of Erlangen-Nuremberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, Germany

DOI: https://doi.org/10.3390/M1081
Journal volume & issue: Vol. 2019, no. 3
p. M1081

Abstract

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(E)-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.

Published in Molbank

ISSN: 1422-8599 (Online)
Publisher: MDPI AG
Country of publisher: Switzerland
LCC subjects: Science: Chemistry: Inorganic chemistry
Website: https://www.mdpi.com/journal/molbank

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Abstract

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