A facile synthesis of aryl iodides via potassium aryltrifluoroborates

Tetrahedron Letters

Volumn 45, Issue 2, 2004, Pages 343-345

  Kabalka, George W ^a   Mereddy, Arjun R ^a  

^a UNIVERSITY OF TENNESSEE   (United States)

Author keywords

Aryl iodide; Iodination; Organoboronic acid; Potassium aryltrifluoroborate

Indexed keywords

BORIC ACID; IODINE DERIVATIVE; OXIDIZING AGENT; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; POTASSIUM DERIVATIVE; SODIUM IODIDE;

ARTICLE; CHEMICAL MODIFICATION; DRUG SELECTIVITY; DRUG SYNTHESIS; IODINATION; QUANTUM YIELD;

EID: 0346996542     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.10.149     Document Type: Article

References (19)

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18. General procedure: To a solution of potassium aryltrifluoroborate (1.00 mmol) in 50% aqueous tetrahydrofuran (5 mL) contained in a round bottomed flask (which was shielded from light), chloramine-T (1.00 mmol) was added followed by sodium iodide (1.05 mmol). The resulting mixture was stirred at room temperature for the required length of time (Table 2.
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