&lt;b&gt;Preparation of diethyl malonate adducts from chalcone analogs containing a thienyl ring&lt;/b&gt;

Budak, Yakup; Gürdere, Meliha Burcu; Keçeci, Meryem; Ceylan, Mustafa

doi:10.4314/bcse.v24i1.52964

Cited by 4 publications

(1 citation statement)

References 14 publications

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“…A doublet at 7.55 ppm corresponds to 4 and 5 th position protons of thiophene ring. These peaks confirm the formation of the compounds [10,11]. The compound formation was confirmed by the recorded H 1 NMR spectra and they reveal the substitution to 2-position of thienyl ring in 2-CTP causing a downfield shift of approximately 0.9 -1 ppm from the substitution to 3-position of thienyl ring in 3-CTP.…”

Section: Growth Of 2-ctp and 3-ctp Single Crystalssupporting

confidence: 66%

Effect of Substituent Position on the Properties of Chalcone Isomer Single Crystals

Gandhimathi¹,

Vinitha²,

Dhanasekaran³

2013

JCPT

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This paper summarizes the synthesis, growth and the effect of the position of the substituent in the thienyl ring and also the properties of the grown chalcone crystals, 2-CTP and 3-CTP. The formation of compound is confirmed by the recorded H 1 NMR spectra. A FT-IR spectrum confirms the presence of all functional groups in both of the crystals. Single crystal XRD reports that even though these two compounds crystallize in monoclinic crystal system, 2-CTP has centrosymmetric P2 1 /c space group and 3-CTP has non-centrosymmetric space group P2 1. Thermal properties of grown crystals analyzed by TG/DTA study explain that the 3-CTP compound is slightly more stable than 2-CTP. The transparency of these isomers in the vis-IR region has been studied. Second and third order nonlinear optical properties of 3-CTP and 2-CTP crystals have been investigated by powder SHG and Z-scan technique respectively.

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Section: Growth Of 2-ctp and 3-ctp Single Crystalssupporting

confidence: 66%

Effect of Substituent Position on the Properties of Chalcone Isomer Single Crystals

Gandhimathi¹,

Vinitha²,

Dhanasekaran³

2013

JCPT

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An Efficient and Environmentally Benign Bentonite–Gold Nanohybrid‐Catalyzed Oxidative Cross‐Coupling of Ketones with Benzylic Primary Alcohols

Maya

Varma

2017

Asian J Org Chem

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An efficient, green and sustainable method for the oxidative C−C coupling of ketones and primary alcohols was developed using an environmentally benign bentonite–gold nanohybrid catalyst. This heterogeneous catalyst affords diverse α,β‐unsaturated ketones in excellent yields under ambient reaction conditions in the presence of Cs2CO3 as weak base. The catalyst is selective, recyclable and only water is produced as the side product. This catalytic system is readily applicable for the gram‐scale synthesis of α,β‐unsaturated ketones.

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Potassium tert‐Butoxide Catalyzed Synthesis and Characterization of Novel 3‐Aryl‐3‐(phenylthio)‐1‐(thiophen‐3‐yl)propan‐1‐one Derivatives

Budak¹

2012

Chin. J. Chem.

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<b>Preparation of diethyl malonate adducts from chalcone analogs containing a thienyl ring</b>

Cited by 4 publications

References 14 publications

Effect of Substituent Position on the Properties of Chalcone Isomer Single Crystals

Effect of Substituent Position on the Properties of Chalcone Isomer Single Crystals

An Efficient and Environmentally Benign Bentonite–Gold Nanohybrid‐Catalyzed Oxidative Cross‐Coupling of Ketones with Benzylic Primary Alcohols

Potassium tert‐Butoxide Catalyzed Synthesis and Characterization of Novel 3‐Aryl‐3‐(phenylthio)‐1‐(thiophen‐3‐yl)propan‐1‐one Derivatives

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