Reactions of aryl ketones and coumarins with iodine (III) tris (trifluoroacetate)
N Fukuyama, H Nishino, K Kurosawa
Index: Fukuyama, Norihiro; Nishino, Hiroshi; Kurosawa, Kazu Bulletin of the Chemical Society of Japan, 1987 , vol. 60, # 12 p. 4363 - 4368
Full Text: HTML
Citation Number: 15
Abstract
The reaction of acetophenones with iodine (III) tris (trifluoroacetate) yields 3′-and/or 2-iodo derivatives, depending upon the substituent on the aromatic ring and the reaction conditions. The reaction was examined by changing the molar ratio of acetophenone versus the reagent, reaction temperature, and solvent. In similar reactions flavanones and coumarins gave iodo derivatives in which iodine is incorporated at various positions ...
Related Articles:
[Dixon, Luke I.; Carroll, Michael A.; Gregson, Thomas J.; Ellames, George J.; Harrington, Ross W.; Clegg, William European Journal of Organic Chemistry, 2013 , # 12 p. 2334 - 2345]
[Dixon, Luke I.; Carroll, Michael A.; Gregson, Thomas J.; Ellames, George J.; Harrington, Ross W.; Clegg, William European Journal of Organic Chemistry, 2013 , # 12 p. 2334 - 2345]
[Dixon, Luke I.; Carroll, Michael A.; Gregson, Thomas J.; Ellames, George J.; Harrington, Ross W.; Clegg, William European Journal of Organic Chemistry, 2013 , # 12 p. 2334 - 2345]
[Boyer, Joseph H.; Natesh, Anbazhagan Synthesis, 1988 , # 12 p. 980 - 981]