Relevant bibliographies by topics / Doebner synthesis

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Academic literature on the topic 'Doebner synthesis'

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

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Journal articles on the topic "Doebner synthesis"

1

Peyrot, Cédric, Matthieu M. Mention, Robin Fournier, et al. "Expeditious and sustainable two-step synthesis of sinapoyl-l-malate and analogues: towards non-endocrine disruptive bio-based and water-soluble bioactive compounds." Green Chemistry 22, no. 19 (2020): 6510–18. http://dx.doi.org/10.1039/d0gc02763d.

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2

Zacuto, Michael J. "Synthesis of Acrylamides via the Doebner–Knoevenagel Condensation." Journal of Organic Chemistry 84, no. 10 (2019): 6465–74. http://dx.doi.org/10.1021/acs.joc.9b00450.

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Zhang, Z. P., L. M. V. Tillekeratne, and Richard A. Hudson. "An unusual product in a Doebner-von Miller quinoline synthesis." Tetrahedron Letters 39, no. 29 (1998): 5133–34. http://dx.doi.org/10.1016/s0040-4039(98)01008-9.

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4

Ghosh, Suman Kr, and Rajagopal Nagarajan. "Total synthesis of actinophenanthroline A via double Doebner–Miller reaction." Tetrahedron Letters 57, no. 36 (2016): 4009–11. http://dx.doi.org/10.1016/j.tetlet.2016.06.045.

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5

N., G. Salunkhe, V. Thakare N., A. Ladole C., and S. Aswar A. "Green synthesis of quinoline-4-carboxylic acid derivatives using silica sulfuric acid as an efficient catalyst." Journal of Indian Chemical Society Vol. 92, Aug 2015 (2015): 1295–98. https://doi.org/10.5281/zenodo.5599012.

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Department of Chemistry, Sant Gadge Baba Amravati University, Amravati-444 602, Maharashtra, India <em>E-mail</em> : aswaranand@gmail.com <em>Manuscript received online 22 October 2014, accepted 16 December 2014</em> Quinoline-4-caboxylic acid derivatives were synthesized in moderate to high yields via one-pot three components Doebner reaction of pyruvic acid, aldehydes and anilines in the presence of silica sulfuric acid as an efficient catalyst, under very mild conditions with excellent yields. The notable advantages of this protocol are work-up procedure is easy and the catalyst can be reco
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6

Halim, Ayu Mutmainnah, Antonius Herry Cahyana, and Rika Tri Yunarti. "One-Pot Synthesis of 2-Phenylquinoline-4-Carboxylic Acid: Iron(III) Trifluoromethanesulfonate Catalysed Doebner Reaction." Key Engineering Materials 907 (January 21, 2022): 97–102. http://dx.doi.org/10.4028/www.scientific.net/kem.907.97.

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Iron (III) trifluoromethanesulfonate [Fe (OTF)3] has been proven to be an effective catalyst in the synthesis of 2-phenylquinoline-4-carboxylic acid by the Doebner reaction using one-pot pyruvic acid, aniline, and benzaldehyde. This method shows attractive characteristics including concise one-pot conditions, high atom economy, very limited energy consumption, and the sequential catalytic process requires only a catalytic (15 mol%) amount of Fe (OTf)3 with short reaction periods (3 h) . Meanwhile, the catalyst was easily recovered from the reaction system and reused smoothly with only a little
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7

Denmark, Scott E., and Srikanth Venkatraman. "On the Mechanism of the Skraup−Doebner−Von Miller Quinoline Synthesis." Journal of Organic Chemistry 71, no. 4 (2006): 1668–76. http://dx.doi.org/10.1021/jo052410h.

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8

Matsugi, Masato, Fujio Tabusa, and Jun-ichi Minamikawa. "Doebner–Miller synthesis in a two-phase system: practical preparation of quinolines." Tetrahedron Letters 41, no. 44 (2000): 8523–25. http://dx.doi.org/10.1016/s0040-4039(00)01542-2.

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9

ZHANG, Z. P., L. M. V. TILLEKERATNE, and R. A. HUDSON. "ChemInform Abstract: An Unusual Product in a Doebner-von Miller Quinoline Synthesis." ChemInform 29, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199840112.

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10

Rioux, Benjamin, Cédric Peyrot, Matthieu M. Mention, Fanny Brunissen, and Florent Allais. "Sustainable Synthesis of p-Hydroxycinnamic Diacids through Proline-Mediated Knoevenagel Condensation in Ethanol: An Access to Potent Phenolic UV Filters and Radical Scavengers." Antioxidants 9, no. 4 (2020): 331. http://dx.doi.org/10.3390/antiox9040331.

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p-Hydroxycinnamic diacids are reaction intermediates of the classical Knoevenagel–Doebner condensation between malonic acid and benzaldehydes. As they are generally obtained in low yields, they remain relatively under-studied and under-exploited. Herein, we developed and optimized a sustainable synthetic procedure allowing the production of these compounds in good to high yields (60–80%) using proline as the catalyst and ethanol as the solvent. Study of their antioxidant and anti-UV activities revealed that these p-hydroxycinnamic diacids were not only potent radical scavengers but also effici
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Book chapters on the topic "Doebner synthesis"

1

Li, Jie Jack. "Doebner quinoline synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_90.

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2

Li, Jie Jack. "Doebner quinoline synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_83.

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Journal articles
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