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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 36, 2006 - Issue 21
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Original Articles

Selective Protection of Carbonyl Compounds as Azines and Their Facile Regeneration

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Pages 3161-3165 | Received 24 Apr 2006, Published online: 24 Nov 2006

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Read on this site (3)

Letcy V. Theresa, M. Shaibuna & K. Sreekumar. (2019) Glucose:urea:NH4Cl low melting mixture for the synthesis of symmetric azines. Synthetic Communications 49:22, pages 3148-3160.
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J. Safari & S. Gandomi-Ravandi. (2011) Highly Efficient Practical Procedure for the Synthesis of Azine Derivatives Under Solvent-Free Conditions. Synthetic Communications 41:5, pages 645-651.
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H. M. Nanjundaswamy & M. A. Pasha. (2007) Rapid, Chemoselective and Facile Synthesis of Azines by Hydrazine/I2 . Synthetic Communications 37:19, pages 3417-3420.
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Articles from other publishers (14)

Dario Perdicchia. (2023) Ionic hydrogenation of azines: An efficient synthesis of 1,2-dialkylhydrazines. Tetrahedron 139, pages 133432.
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Rakesh Mondal, Amit Kumar Guin, Subhajit Chakraborty & Nanda D. Paul. (2022) Iron-Catalyzed Metal–Ligand Cooperative Approach toward Sustainable Synthesis of Azines and N -Acylhydrazones in Air . The Journal of Organic Chemistry 87:5, pages 2921-2934.
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Miguel A. Valle-Amores, Matías Blanco, Stefano Agnoli, Alberto Fraile & José Alemán. (2022) Oxidized multiwalled nanotubes as efficient carbocatalyst for the general synthesis of azines. Journal of Catalysis 406, pages 174-183.
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Jugal Kishore, Subramanian Thiyagarajan & Chidambaram Gunanathan. (2019) Ruthenium( ii )-catalysed direct synthesis of ketazines using secondary alcohols . Chemical Communications 55:31, pages 4542-4545.
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Fenhua Zhang, Weilu Wang, Shixiang Hu, Xiaotong Ma, Wenliang Gao, Rihong Cong & Tao Yang. (2017) A nanosized aluminoborate (PKU-5) with Cr-centered octahedral framework: Solid-phase synthesis, characterizations and catalytic ammoximation of cyclohexanone to cyclohexanone azine. Applied Catalysis A: General 531, pages 60-68.
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Zai-Gang Luo, Peng Liu, Yu-Yu Fang, Xue-Mei Xu, Cheng-Tao Feng, Zhong Li, Xiao-Mei Zhang & Jie He. (2016) Cs2CO3-mediated decomposition of N-tosylhydrazones for the synthesis of azines under mild conditions. Research on Chemical Intermediates 43:2, pages 1139-1148.
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R. Arulmani, R. Balachander, P. Vijaya & K.R. Sankaran. (2015) Spectral and conformational studies on 3-pyridinealdazine by DFT approach. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 138, pages 660-666.
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P. Vijaya & K.R. Sankaran. (2015) A combined experimental and DFT study of a novel unsymmetrical azine 2-(4-methoxybenzylidene)-1-(1-(4-isobutylphenyl) ethylidene) hydrazine. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 138, pages 460-473.
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K. Ravi, B. Krishnakumar & M. Swaminathan. (2012) An Efficient Protocol for the Green and Solvent-Free Synthesis of Azine Derivatives at Room Temperature Using BiCl 3 -Loaded Montmorillonite K10 as a New Recyclable Heterogeneous Catalyst . ISRN Organic Chemistry 2012, pages 1-9.
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Davood Habibi, Mohammad Ali Zolfigol, Ali Reza Faraji & Payam Rahmani. (2011) Selective conversion of C=N bonds to their corresponding carbonyl compounds by the tribromoisocyanuric acid/wet SiO2 system as a novel reagent. Monatshefte für Chemie - Chemical Monthly 143:5, pages 809-814.
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B. Krishnakumar & M. Swaminathan. (2011) An expeditious and solvent free synthesis of azine derivatives using sulfated anatase–titania as a novel solid acid catalyst. Catalysis Communications 16:1, pages 50-55.
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. (2008) Efficient, Catalytic and Oxidative Deoximation of Aldoximes and Ketoximes by Ferric Nitrate and Catalytic Amounts of Bromide Ion. Bulletin of the Korean Chemical Society 29:12, pages 2496-2498.
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Hossein Eshghi & Mosayyeb Hosseini. (2013) Selective and Convenient Protection of Aldehydes as Azines under Solvent‐Free Conditions. Journal of the Chinese Chemical Society 55:3, pages 636-638.
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H. M. Nanjundaswamy & M. A. Pasha. (2007) Selective Protection of Carbonyl Compounds as Azines and Their Facile Regeneration.. ChemInform 38:11.
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