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	<dc:title xml:lang="en-US">Newer chalcone scaffolds with reactive functional groups: Process, spectral and single crystal XRD studies</dc:title>
	<dc:creator>Borane, Niteen</dc:creator>
	<dc:creator>Deshmukh, Amar Ghanshyam</dc:creator>
	<dc:creator>Oza, Nidhi Harnesh</dc:creator>
	<dc:creator>Boddula, Rajamouli</dc:creator>
	<dc:creator>Patel, Paresh Narayan</dc:creator>
	<dc:subject xml:lang="en-US">Nitrile</dc:subject>
	<dc:subject xml:lang="en-US">Chalcone</dc:subject>
	<dc:subject xml:lang="en-US">Pyrrolidine</dc:subject>
	<dc:subject xml:lang="en-US">Heterocycle</dc:subject>
	<dc:subject xml:lang="en-US">Single-crystal XRD</dc:subject>
	<dc:subject xml:lang="en-US">4-Formylbenzonitrile</dc:subject>
	<dc:description xml:lang="en-US">Chalcones are versatile scaffolds for the synthesis of various heterocyclic systems with commercial utility. This work describes the synthesis of five novel chalcone derivatives. Syntheses were performed by a simple one-pot, straightforward Claisen-Schmidt condensation catalyzed with pyrrolidine and KOH. The chalcones were prepared by condensation of 4-formylbenzonitrile with different aromatic ketones at room temperature. The structures of all compounds have been investigated by FT-IR, NMR, and HR-MS spectroscopy. In addition, one chalcone structure was characterized by single-crystal XRD study. Crystal data for C21H15NO2 (Ch2): monoclinic, space group P21/c (no. 14), a = 6.5694(3) Å, b = 33.2697(15) Å, c = 7.4516(4) Å, β = 97.563(2)°, V = 1614.47(14) Å3, Z = 4, T = 293(2) K, μ(MoKα) = 0.083 mm-1, Dcalc = 1.289 g/cm3, 16000 reflections measured (4.898° ≤ 2Θ ≤ 49.99°), 2822 unique (Rint = 0.0249, Rsigma = 0.0196) which were used in all calculations. The final R1 was 0.0484 (I &amp;gt; 2σ(I)) and wR2 was 0.1257 (all data). The absorption maxima of all novel products were evaluated by UV-visible spectroscopy. These well-established structures of all newly prepared chalcone scaffolds with reactive functional groups (i.e. nitrile and 2-propenone) can be exploited as a crucial intermediate in the synthesis of new heterocyclic scaffolds with fluorescence and other applications.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2023-06-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/2405</dc:identifier>
	<dc:identifier>10.5155/eurjchem.14.2.297-302.2405</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 14 No. 2 (2023): June 2023; 297-302</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/2405/2747</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2023 Authors</dc:rights>
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