Relevant bibliographies by topics / Erlenmeyer Azlactone Synthesis

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Erlenmeyer Azlactone Synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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Journal articles on the topic "Erlenmeyer Azlactone Synthesis"

1

Karade, N. N., S. G. Shirodkar, B. M. Dhoot, and P. B. Waghmare. "Montmorillonite K-10 mediated Erlenmeyer synthesis of 4-arylmethylene-2-phenyl-5(4H)-oxazolones." Journal of Chemical Research 2005, no. 1 (2005): 46–47. http://dx.doi.org/10.3184/0308234053431176.

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Aromatic aldehydes and hippuric acid in acetic anhydride undergoes classical Erlenmeyer synthesis in the presence of a catalytic amount of Montmorillonite K-10 to afford the corresponding azlactones in excellent yields with high selectivity. The azlactone formation does not proceed in the absence of either acetic anhydride or Montmorillonite.
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2

Shafiee, Behnaz, Laleh Hadian, and Ahmad R. Khosropour. "An innovation for development of Erlenmeyer–Plöchl reaction and synthesis of AT-130 analogous: a new application of continuous-flow method." RSC Advances 6, no. 24 (2016): 19861–66. http://dx.doi.org/10.1039/c6ra00301j.

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3

Chandrasekhar, Sosale, and Phaneendrasai Karri. "Aromaticity in azlactone anions and its significance for the Erlenmeyer synthesis." Tetrahedron Letters 47, no. 32 (2006): 5763–66. http://dx.doi.org/10.1016/j.tetlet.2006.06.006.

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4

Chandrasekhar, Sosale, and Phaneendrasai Karri. "Erlenmeyer azlactone synthesis with aliphatic aldehydes under solvent-free microwave conditions." Tetrahedron Letters 48, no. 5 (2007): 785–86. http://dx.doi.org/10.1016/j.tetlet.2006.11.174.

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5

Verma, Tarawanti, Manish Sinha, and Nitin Bansal. "Synthesis of Novel 1,2-Dihydro-1,2,4-Triazin-6(5H)-one Derivatives as Anticancer Agents." Current Bioactive Compounds 16, no. 7 (2020): 1116–31. http://dx.doi.org/10.2174/1573407215666191022123310.

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Introduction: Cancer is still an untreatable disease and the second leading cause of death globally. The heterocyclic compounds have always played a major role in the anticancer drug discovery program. 1,2,4-Triazine-6-ones is a heterocyclic privileged structure with diversified activities. In the presented study, 21 novel 2,5-disubstituted-3-phenyl-1,2-dihydro-1,2,4-triazin-6 (5H)-one derivatives (13(a-k), 18(a-j) and 21(a1-a4, b)) have been synthesized and tested for their anticancer activity. Methods: The 2,5-disubstituted-3-phenyl-1,2-dihydro-1,2,4-triazin-6(5H)-one derivatives (13(a-k), 1
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6

Parveen, Mehtab, Faheem Ahmad, Ali Mohammed Malla, Shaista Azaz, Manuela Ramos Silva, and P. S. Pereira Silva. "[Et3NH][HSO4]-mediated functionalization of hippuric acid: an unprecedented approach to 4-arylidene-2-phenyl-5(4H)-oxazolones." RSC Advances 5, no. 65 (2015): 52330–46. http://dx.doi.org/10.1039/c5ra09290f.

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7

Jagadale, Megha, Altafhusen Naikwade, Rajashri Salunkhe, Mohan Rajmane, and Gajanan Rashinkar. "An ionic liquid gel: a heterogeneous catalyst for Erlenmeyer–Plochl and Henry reactions." New Journal of Chemistry 42, no. 13 (2018): 10993–1005. http://dx.doi.org/10.1039/c8nj00367j.

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8

Zhou, Baocheng, and Wenxing Chen. "The Zwitterionic Imidazolium Salt: First Used for Synthesis of 4-Arylidene-2-phenyl-5(4H)-oxazolones under Solvent-Free Conditions." Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/280585.

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The zwitterionic imidazolium salt was prepared and characterized by1H NMR. It was first used for synthesis of azlactones via Erlenmeyer synthesis from aromatic aldehydes and hippuric acid under solvent-free conditions. It was found that aldehyde substituents play an important role in these reactions. Better conversions and therefore higher isolated yields were observed when electron-withdrawing groups (EWG-) were present in the aromatic aldehyde. Opposite results were shown when electron-donating groups (EDG-) were present in the aromatic aldehyde. However, azlactones were obtained in moderate
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9

El-Mekabaty, Ahmed. "ChemInform Abstract: Erlenmeyer Azlactones. Synthesis, Reactions and Biological Activity." ChemInform 44, no. 34 (2013): no. http://dx.doi.org/10.1002/chin.201334216.

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10

Kiyani, Hamzeh, and Shiva Aslanpour. "Synthesis of Erlenmeyer-Plöchl Azlactones Promoted by 5-Sulfosalicylic Acid." HETEROCYCLES 94, no. 7 (2017): 1314. http://dx.doi.org/10.3987/com-17-13711.

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Dissertations / Theses on the topic "Erlenmeyer Azlactone Synthesis"

1

Karri, Phaneendrasai. "Mechanistic And Synthetic Investigations On Carboxylic Anhydrides And Their Analogs." Thesis, 2008. https://etd.iisc.ac.in/handle/2005/1058.

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This thesis reports diverse synthetic and mechanistic studies in six chapters, as summarized below. Chapter 1. Revised mechanism and improved methodology for the perkin condensation.1 The generally accepted mechanism for the well-known Perkin condensation is unviable for at least two reasons: (1) the normally employed base, acetate ion, is too weak to deprotonate acetic anhydride (Ac2O, the substrate); and (2) even were Ac2O to be derprotonated , its anion would rapidly fragment to ketene and acetate ion at the high temperatures employed for the reaction. It has proved in this study that the
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2

Karri, Phaneendrasai. "Mechanistic And Synthetic Investigations On Carboxylic Anhydrides And Their Analogs." Thesis, 2008. http://hdl.handle.net/2005/1058.

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This thesis reports diverse synthetic and mechanistic studies in six chapters, as summarized below. Chapter 1. Revised mechanism and improved methodology for the perkin condensation.1 The generally accepted mechanism for the well-known Perkin condensation is unviable for at least two reasons: (1) the normally employed base, acetate ion, is too weak to deprotonate acetic anhydride (Ac2O, the substrate); and (2) even were Ac2O to be derprotonated , its anion would rapidly fragment to ketene and acetate ion at the high temperatures employed for the reaction. It has proved in this study that the P
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Book chapters on the topic "Erlenmeyer Azlactone Synthesis"

1

Li, Jie Jack. "Erlenmeyer–Plöchl azlactone synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_95.

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2

Li, Jie Jack. "Erlenmeyer–Plöchl azlactone synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_88.

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