A mild and simple regioselective iodination of activated aromatics with iodine and catalytic ceric ammonium nitrate
B Das, M Krishnaiah, K Venkateswarlu, VS Reddy
Index: Das, Biswanath; Krishnaiah, Maddeboina; Venkateswarlu, Katta; Reddy, V. Saidi Tetrahedron Letters, 2007 , vol. 48, # 1 p. 81 - 83
Full Text: HTML
Citation Number: 53
Abstract
Aromatic iodo compounds are important intermediates for the synthesis of various pharmaceutical and bioactive compounds. 1 They are also useful in metal-catalyzed cross coupling reactions, such as Heck, Stille and Negishi reactions which are utilized in C–C and C–N bond formation. 2 However, direct iodination of aromatic compounds is difficult due to the low electrophilicity of molecular iodine compared to that of molecular chlorine and bromine. Generally, ...
Related Articles:
Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions
[Morice, Christophe; Domostoj, Mathias; Briner, Karin; Mann, Andre; Suffert, Jean; Wermuth, Camille-Georges Tetrahedron Letters, 2001 , vol. 42, # 37 p. 6499 - 6502]
Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions
[Morice, Christophe; Domostoj, Mathias; Briner, Karin; Mann, Andre; Suffert, Jean; Wermuth, Camille-Georges Tetrahedron Letters, 2001 , vol. 42, # 37 p. 6499 - 6502]