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(E)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one

1
Department of Chemistry and Pharmacy, Institute of Organic Chemistry I, University of Erlangen-Nuremberg, Nikolaus-Fiebiger-Str. 10, 91058 Erlangen, Germany
2
Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki St., Rostov on Don 344090, Russia
*
Author to whom correspondence should be addressed.
Molbank 2019, 2019(3), M1081; https://doi.org/10.3390/M1081
Received: 19 August 2019 / Revised: 16 September 2019 / Accepted: 17 September 2019 / Published: 18 September 2019
(This article belongs to the Special Issue Molecules from Side Reactions)
(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. View Full-Text
Keywords: oxazole; furan; RORC reaction; (E,Z)-isomerization oxazole; furan; RORC reaction; (E,Z)-isomerization
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MDPI and ACS Style

Sawengngen, N.; Kolodina, A.A.; Serdyuk, O.V. (E)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one. Molbank 2019, 2019, M1081. https://doi.org/10.3390/M1081

AMA Style

Sawengngen N, Kolodina AA, Serdyuk OV. (E)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one. Molbank. 2019; 2019(3):M1081. https://doi.org/10.3390/M1081

Chicago/Turabian Style

Sawengngen, Nattawut; Kolodina, Alexandra A.; Serdyuk, Olga V. 2019. "(E)-4-(3-Phenylisoxazol-5-yl)but-3-en-2-one" Molbank 2019, no. 3: M1081. https://doi.org/10.3390/M1081

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