Relevant bibliographies by topics / Phenacyi bromide

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Phenacyi bromide'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Phenacyi bromide"

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Neelam, Dhakar, Ojha Swati, Lal Jat Jawahar, and L. Talesara G. "Synthesis and characterization of some 3-N-alkoxyphthalimido-5-arylidene-2- { [ 4-( 4-substituted phenyl)-1 ,3-thiazol-2-yl]imino }-1 ,3-thiazolidin-4-ones." Journal of Indian Chemical Society Vol. 85, June 2008 (2008): 660–64. https://doi.org/10.5281/zenodo.5816939.

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Synthetic Organic Chemistry Research Laboratory, Department of Chemistry, M. L. Sukhadia University. Udaipur-313 001, Rajasthan, India <em>E-mail :</em> gtalesara@yahoo.com <em>Manuscript received 17 July 2006. revised 6 September 2007, accepted 15 April 2008</em> 4-Chloro/methyl phenacyl bromide 1a-b reacted with thiourea to furnish 2-amino thiazole 2a-b through Hantzsch&#39;s process, which were converted to their thlazolidinone derivatives 4a-b, by the reaction of corresponding thiazolyl thiourea 3a-b with chloroacetic acid in the presence of sodium acetate. Subsequent treatment of 4a-b wit
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M., KRISHNA PILLAY, and M. MAZHAR NAZEEB KHAN S. "Kinetics and Mechanism of Oxidation of Phenacyl Bromide by Alkaline Hexacyanoferrate(III)." Journal of Indian Chemical Society Vol. 70, Mar 1993 (1993): 209–10. https://doi.org/10.5281/zenodo.5913740.

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Department of Chemistry, Bharathidasan University, Tiruchirapalli-620 024 <em>Manuscript received 14 November 1991, revised 9 November 1992, accepted 7 January 1993</em> Kinetics of oxidation a few phenacyl bromides in aqueous acetonitri&#39;e by hexacyanoferrate(III) at 10<sup>&deg;</sup>&nbsp;,has been studied. The reaction is first order in oxidant, phenacyl bromide and hydroxide. The enolate of pheoacyl bromide and ferricyaoide are the reactive species. A suitable mechanism is suggested. Substituent effect is also analysed.
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Basha, Shaik Firoj, and Shaik Anwar. "A Three Component Protocol for the Synthesis of Aziridines using BF3·(OEt)2." Asian Journal of Chemistry 32, no. 5 (2020): 1001–6. http://dx.doi.org/10.14233/ajchem.2020.22315.

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Synthesis of N-(1R,2S)-2-(bromo-3-oxo-1,3-diphenylpropyl)-4-methylbenzene sulfonamide and N-(1R,2S)-(2-bromo-3-oxo-1,3-diphenylpropyl)-4-methylbenzene sulfonamide was carried out by a three component reaction using phenacyl bromide, p-toluenesulfonamide and carboxyaldehyde in presence of mild Lewis acid such as BF3·(OEt)2 in dichloromethane. The synthetic utility of this protocol was carried out with syn-isomer to yield corresponding cis-aziridines. This protocol was operationally simple for a wide variety of substituted carboxaldehydes and substituted phenacyl bromides.
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Jwad, Rasha, Adnan Mohammed, and Mehdi Shihab. "SYNTHESIS OF 1,2,3-TRIAZOLES BASED ON PHENACYL AZIDE DERIVATIVES VIA CLICK CHEMISTRY." Iraqi Journal of Science 53, no. 3 (2024): 487–94. http://dx.doi.org/10.24996/iraqijournalofscience.v53i3.12746.

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Etherification of n-hexanol, n-heptanol and n-octanol with propargyl bromide in the presence of sodium hydroxide in DMF afforded the terminal alkynes (2) a, b and c. Phenacyl bromide, p-bromophenacyl bromide and p-phenylphenacyl bromide were converted to corresponding azides (4) a, b and c respectively by traditional SN2 reaction of the mentioned bromides and sodium azide in DMF. The cycloaddition of the propargyl ethers (2) with the prepared organic azides (4) using click conditions gave the target 1,4-disubstituted 1,2,3- triazoles (5)-(7) in good yields. All the synthesized triazoles were c
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B., HARI KISHAN, and V. SUNDARAM E. "Anomalous Kinetic Behaviour of Methyl and Methoxy Derivatives on the Oxidation of Phenacyl Bromides by Cerium(IV) in Sulphuric Acid Medium." Journal of Indian Chemical Society Vol. 62, Sep 1985 (1985): 654–56. https://doi.org/10.5281/zenodo.6322015.

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Department of Chemistry, Kakatiya University, Warangal-506 009 <em>Manuscript received 23 May 2985, accepted 11 September 1985</em> The kinetics of cerium(IV) oxidation of p-methyl- and <em>p</em>-methoxy-phenacyl bro&shy;mides have been investigated in 40-70% (v/v) acetic acid containing varying concentra&shy;tions of sulphuric acid. The reactions are first<em> </em>order with<em> </em>respect to [oxidant] as well as [substrate]. The reactions are acid-catalysed and the absence of water molecule participation is indicated and discussed through Hammett&#39;s acidity and Bunnett&#39;s plots. Th
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B., HARI KISHAN, and V. SUNDARAM B. "Kinetics of Oxidation of Phenacyl Halides by Vanadium( v) in Sulphuric and Perchloric Acid Media." Journal of Indian Chemical Society Vol. 66, Jun 1989 (1989): 363–64. https://doi.org/10.5281/zenodo.5958301.

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Department of Chemistry, Kakatiya University, Warangal-506&nbsp;009 <em>Manuscript received </em>8 <em>July 1988, revised 30 January 1989, accepted 18 </em>April.<em>1989</em> A kinetic study of oxidation of phenacyl halides, namely, phenacyl chloride, phenacyl bromide and phenacyl iodide by vanadium(v) in acid medium, obeys first order with respect to [oxidant] and [substrata]. The reactions are acid-catalysed and various hypothesis for the mechanism of acid catalysis have been tested. The different reactivity of phenacyl halides is explained on the basis of different Inductive effect felt by
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7

Lomov, D. A., M. G. Abramyants, O. O. Zaporozhets, and T. M. Pekhtereva. "Quaternization of Methyl Picolinate with Some Phenacyl Bromides. Synthesis of DL-Baikiain Alkaloid." Журнал общей химии 94, no. 1 (2024): 105–12. http://dx.doi.org/10.31857/s0044460x24010095.

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By fusing methyl picolinate with phenacyl bromides, the corresponding phenacyl salts were obtained, cyclization of which in acetic anhydride led to previously undescribed 3-aryl-1H-pyrido[2,1-c][1,4]oxazinium bromides. Reduction of the quaternary salts of methyl picolinate followed by acid hydrolysis leads to the alkaloid DL-baikiain.
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Abu-Shanab, Fathi A. "Synthesis of 2,3,4,6-Tetrasubstituted Pyridines as Precursors to Bicycles and Polycycles." Journal of Chemical Research 23, no. 7 (1999): 430–31. http://dx.doi.org/10.1177/174751989902300713.

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Ammonium 1,1,3-tricyano-2-methylprop-2-enide 1a and sodium 2-amino-1,1,3-tricyanoprop-2-enide 1b are treated with H2S in absolute ethanol to afford 3,4,6-trisubstituted pyridine-2(1 H)-thione 3a,b; their structures are confirmed by reaction with phenacyl bromide to give 4a,b; also 3a,b reacts with DMFDMA to give 6a,b, and on treatment of 6a with phenacyl bromide affords 8; reaction of 4b with DMFDMA gave 9 while methylation of 3a,b by methyl iodide in ethanolic sodium hydroxide gives 10a,b.
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Baghdadchi, Jamil, Albert P. Chan, and James H. Hutchinson. "Reactions of substituted phenacyl bromides with various bases:p-methyl- andp-methoxyphenacyl bromide. II." Journal of Heterocyclic Chemistry 25, no. 3 (1988): 973–74. http://dx.doi.org/10.1002/jhet.5570250351.

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VlJAI, N. PATHAK, K. GOYAL MAHENDRA, JAIN MEENAKSHI, and C. JOSHI KRISHNA. "Synthesis of some New Fluorine containing Oxazoles, Oxadiazoles, Thiadiazoles and Triazines." Journal of Indian Chemical Society Vol.70, Jun 1993 (1993): 539–42. https://doi.org/10.5281/zenodo.5913958.

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Department of Chemistry, University of Rajasthan, Jaipur-300 004 <em>Manuscript received 31 March 1992, revised 16 October 1992, accepted 8 February 1993</em> Treatment of fluorine containing phenacyl bromides with urea or substituted arylureas afforded the corresponding 2-(amino/<em>N</em>-arylamino)-4-(fluoroaryl)oxazoles, and with ammonium acetate in glacial acetic acid yielded 2-methyl- 4-(fluoroaryl)oxazoles. Fluorinated arylglyoxals on refluxing with semicarbazide or thiosemicarbazide afforded arylglyoxalsemicarbazones/or thiosemicarbazones, cyclisation of these with potassium carbonate
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Dissertations / Theses on the topic "Phenacyi bromide"

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郭仲鎧. "Formation of Homoallylic Bromohydrins in Indium-Mediated Allylation Reactions of Phenacyl Bromides in Aqueous Solution." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/51319336273722877652.

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碩士<br>國立彰化師範大學<br>化學系<br>102<br>Recently, we focused on green chemistry, so we used water as our major solvent. Because water is readily available, safe, and environmentally benign. Our study is about carrying out indium-mediated allylation reactions of phenacyl bromides in aqueous solution that form homoallytic bromohydrins We can get high yields and functional tolerance in our method. Homoallylic broniohydrins should be useful in organic synthesis. In our study by employing subsequent base treatment, the homoallylic bromohydrins were converted to allyhc epoxides. And the process has been use
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Book chapters on the topic "Phenacyi bromide"

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Dell, C. P. "Using Phenacyl Bromide." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00017.

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Dell, C. P. "Using Phenacyl Bromide Under Phase-Transfer Conditions." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00018.

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Shimizu, T., and N. Kamigata. "Reaction of Phenacyl Bromides with Selenium Powder." In Sulfur, Selenium, and Tellurium. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-039-01196.

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Lindsley, C. W., and M. E. Layton. "Synthesis from Phenacyl Bromides and 3-Methylisothiosemicarbazides." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00572.

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Kumar Jangid, Dinesh, and Surbhi Dhadda. "Phenacyl Bromide: An Organic Intermediate for Synthesis of Five- and Six-Membered Bioactive Heterocycles." In Heterocycles - Synthesis and Biological Activities. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.88243.

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Conference papers on the topic "Phenacyi bromide"

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Pogrebnoi, Vsevolod, Serghei Pogrebnoi, and Fliur Macaev. "The alkylation of the amides of dehydroabietic acid." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab08.

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In this abstract is being discussed the synthesis of new substituted amides of dehydroabietic acid with different bromides in system K2CO3/DMF. It is known fact that many compounds, such as famous isatine 1, have the amide group in its molecule. There is no point in talking about it, because everything is known regarding chemical properties. However, what if there are two amide groups in the molecule at once? Let us see… For our investigation, we used the model of well-known alkylation reaction [1]. As starting material, we used two types of bromide: aliphatic and aromatic – bromoacetone [2] a
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