Relevant bibliographies by topics / Solvent-free Knoevenagel

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Academic literature on the topic 'Solvent-free Knoevenagel'

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

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Journal articles on the topic "Solvent-free Knoevenagel"

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HOSSEINI-SARVARI, Mona, Hashem SHARGHI, and Samane ETEMAD. "Solvent-free Knoevenagel Condensations over TiO2." Chinese Journal of Chemistry 25, no. 10 (2007): 1563–67. http://dx.doi.org/10.1002/cjoc.200790288.

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Pillai, Manoharan Karuppiah, Sooboo Singh, and Sreekanth B. Jonnalagadda. "Solvent-Free Knoevenagel Condensation over Cobalt Hydroxyapatite." Synthetic Communications 40, no. 24 (2010): 3710–15. http://dx.doi.org/10.1080/00397910903531714.

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3

Alok, Kumar Mitra, Karchaudhuri Nilay, and De Aparna. "Solvent-free Knoevenagel condensation reaction under microwave irradiation exploiting a new reagent : antimony trichloride." Journal of Indian Chemical Society Vol. 82, Feb 2005 (2005): 177–79. https://doi.org/10.5281/zenodo.5825122.

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Department of Chemistry, University of Calcutta, 92, Acharya Prafulla Chandra Road, Kolkata-700 009, India Department of Chemistry, Barrackpore Rastraguru Surendranath College, Barrackpore-700 120, India Deshabandhu Mahavidyalaya, Chittaranjan, Burdwan-713 331, India <em>Manuscript received 14 October 2003, revised 14 September 2004, accepted 17 September 2004</em> A rapid microwave-assisted Knoevenagel condensation exploiting antimony trichloride under solvent-free condition is reported. Several aromatic aldehydes condense with malononitrile and ethyl cyanoacetate within a few minutes in high
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4

Ramaiah, Manjunatha M., Nanjunda Swamy Shivananju, and Priya Babu Shubha. "A Facile, Efficient and Solvent-Free Titanium (IV) Ethoxide Catalysed Knoevenagel Condensation of Aldehydes and Active Methylenes." Letters in Organic Chemistry 17, no. 2 (2020): 107–15. http://dx.doi.org/10.2174/1570178616666190401194641.

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: Titanium ethoxide has been employed as a novel and efficient reagent for the Knoevenagel condensation of aldehydes with active methylenes such as diethyl malonate and ethyl cyanoacetate under solvent free conditions to afford substituted olefins in high to excellent yields. The reaction is suitable for a variety of aromatic, aliphatic and heteroaromatic aldehydes with various active methylenes. Parallel to this, microwave irradiation has been utilized to achieve improved reaction rates and enhanced yields. Herein, we illustrated a convenient method for the preparation of α,β-unsaturated comp
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5

Trotzki, Ronald, Markus M. Hoffmann, and Bernd Ondruschka. "Studies on the solvent-free and waste-free Knoevenagel condensation." Green Chemistry 10, no. 7 (2008): 767. http://dx.doi.org/10.1039/b801661e.

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6

Ma, Lufang, Xiaoning Wang, Dongsheng Deng, Feng Luo, Baoming Ji, and Jian Zhang. "Five porous zinc(ii) coordination polymers functionalized with amide groups: cooperative and size-selective catalysis." Journal of Materials Chemistry A 3, no. 40 (2015): 20210–17. http://dx.doi.org/10.1039/c5ta06248a.

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Zhai, Zhi-Wei, Shuang-Hua Yang, Ya-Ru Lv, Chen-Xia Du, Lin-Ke Li, and Shuang-Quan Zang. "Amino functionalized Zn/Cd-metal–organic frameworks for selective CO2 adsorption and Knoevenagel condensation reactions." Dalton Transactions 48, no. 12 (2019): 4007–14. http://dx.doi.org/10.1039/c9dt00391f.

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8

Wan, Jie-Ping, Yanfeng Jing, Yunyun Liu, and Shouri Sheng. "Metal-free synthesis of cyano acrylates via cyanuric chloride-mediated three-component reactions involving a cascade consists of Knoevenagel condensation/cyano hydration/esterification." RSC Adv. 4, no. 109 (2014): 63997–4000. http://dx.doi.org/10.1039/c4ra13826k.

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9

Dou, Ming-Yu, Dan-Dan Zhong, Xian-Qiang Huang, and Guo-Yu Yang. "Imidazole-induced self-assembly of polyoxovanadate cluster organic framework for efficient Knoevenagel condensation under mild conditions." CrystEngComm 22, no. 24 (2020): 4147–53. http://dx.doi.org/10.1039/d0ce00660b.

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Three new polyoxovanadates have been made, one of them displays highly efficient heterogeneous solvent-free catalytic activity and excellent recyclability in the Knoevenagel condensation at room temperature.
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10

Jain, Kavita, Saikat Chaudhuri, Kuntal Pal, and Kalpataru Das. "The Knoevenagel condensation using quinine as an organocatalyst under solvent-free conditions." New Journal of Chemistry 43, no. 3 (2019): 1299–304. http://dx.doi.org/10.1039/c8nj04219e.

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Dissertations / Theses on the topic "Solvent-free Knoevenagel"

1

Makhanya, Nokubonga Prudence. "Solvent-free Knoevenagel condensation over supported mixed metal oxides catalysts." Thesis, 2017. http://hdl.handle.net/10321/2667.

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Submitted in the fulfillment of the requirement for the Master's Degree in Chemistry,Durban University of Technology, 2017.<br>Knoevenagel condensation reaction is a useful protocol for the formation of C=C bond in organic synthesis. This protocol is extensively utilized by synthetic chemist to generate dynamic intermediates or end-products such as perfumes, polymers, pharmaceuticals and calcium antagonists. The reaction is catalyzed by bases such as ammonia, primary and secondary amines, quaternary ammonium salts, Lewis acids, catalysts containing acid-base sites, which are carried out under
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