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Original Articles

1,3-DIBROMO-5,5-DIMETHYLHYDANTOIN AS AN EFFICIENT AND CHEMOSELECTIVE AGENT FOR THE REGENERATION OF CARBONYL COMPOUNDS FROM SEMICARBAZONES AND OXIMES

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Pages 484-490 | Received 21 Feb 2006, Published online: 18 Feb 2009

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Behrooz Maleki. (2015) Solvent-free Synthesis of 2,4,6-Triarylpyridine Derivatives Promoted by 1,3-Dibromo-5,5-dimethylhydantoin. Organic Preparations and Procedures International 47:2, pages 173-178.
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Articles from other publishers (5)

ABBAS AMINI MANESH & BEHZAD SHIRMARDI SHAGHASEMI. (2015) K3[Fe(CN)6].3H2O supported on silica gel: An efficient and selective reagent for the cleavage of oximes to their corresponding carbonyl compounds in aqueous medium. Journal of Chemical Sciences 127:3, pages 493-497.
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. 2014. Greene's Protective Groups in Organic Synthesis. Greene's Protective Groups in Organic Synthesis 554 685 .
Serena Perrone, Francesca Rosato, Antonio Salomone & Luigino Troisi. (2013) Synthesis and reactivity of trifluoromethyl substituted oxaziridines. Tetrahedron 69:19, pages 3878-3884.
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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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Ardeshir Khazaei & Amin Rostami. (2007) 1,3‐Dibromo‐5,5‐dimethylhydantoin as an Efficient and Chemoselective Agent for the Regeneration of Carbonyl Compounds from Semicarbazones and Oximes.. ChemInform 38:3.
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