4-{[(1-Phenyl-1H-pyrazol-3-yl)oxy]methyl}-1,3-dioxolan-2-one

Gyte Vilkauskaite; Wolfgang Holzer; Algirdas Sackus

doi:10.3390/M786

4-{[(1-Phenyl-1H-pyrazol-3-yl)oxy]methyl}-1,3-dioxolan-2-one

Gyte Vilkauskaite (Corresponding author)
, Wolfgang Holzer
, Algirdas Sackus

Publications: Contribution to journal › Article › Peer Reviewed

Abstract

The title compound was obtained by the reaction of tosylated glycerol carbonate with 1-phenyl-1H-pyrazol-3-ol in a good 71% yield. Detailed spectroscopic data (1H-NMR, 13C-NMR, 15N-NMR, IR, MS) are presented.

Original language	English
Number of pages	4
Journal	Molbank
Volume	2012
Issue number	4
DOIs	https://doi.org/10.3390/M786
Publication status	Published - 2012

Austrian Fields of Science 2012

301207 Pharmaceutical chemistry

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http://phaidra.univie.ac.at/o:588059Licence: CC BY 3.0

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@article{9fa5dd28cfa048bfbd637880cf3eff73,

title = "4-\{[(1-Phenyl-1H-pyrazol-3-yl)oxy]methyl\}-1,3-dioxolan-2-one",

abstract = "The title compound was obtained by the reaction of tosylated glycerol carbonate with 1-phenyl-1H-pyrazol-3-ol in a good 71\% yield. Detailed spectroscopic data (1H-NMR, 13C-NMR, 15N-NMR, IR, MS) are presented.",

author = "Gyte Vilkauskaite and Wolfgang Holzer and Algirdas Sackus",

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T1 - 4-{[(1-Phenyl-1H-pyrazol-3-yl)oxy]methyl}-1,3-dioxolan-2-one

AU - Vilkauskaite, Gyte

AU - Holzer, Wolfgang

AU - Sackus, Algirdas

N1 - ***<REP_Import><OA_Full_2013>158313.28</OA_Full_2013></REP_Import>***

PY - 2012

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N2 - The title compound was obtained by the reaction of tosylated glycerol carbonate with 1-phenyl-1H-pyrazol-3-ol in a good 71% yield. Detailed spectroscopic data (1H-NMR, 13C-NMR, 15N-NMR, IR, MS) are presented.

AB - The title compound was obtained by the reaction of tosylated glycerol carbonate with 1-phenyl-1H-pyrazol-3-ol in a good 71% yield. Detailed spectroscopic data (1H-NMR, 13C-NMR, 15N-NMR, IR, MS) are presented.

U2 - 10.3390/M786

DO - 10.3390/M786

M3 - Article

SN - 1422-8599

VL - 2012

JO - Molbank

JF - Molbank

IS - 4

ER -

4-{[(1-Phenyl-1H-pyrazol-3-yl)oxy]methyl}-1,3-dioxolan-2-one

Abstract

Austrian Fields of Science 2012

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