TY - JOUR T1 - Understanding sulfone behavior in palladium-catalyzed domino reactions with aryl iodides. AU - Alonso,Inés, AU - Alcamí,Manuel, AU - Mauleón,Pablo, AU - Carretero,Juan C, PY - 2006/4/6/pubmed PY - 2006/4/6/medline PY - 2006/4/6/entrez SP - 4576 EP - 83 JF - Chemistry (Weinheim an der Bergstrasse, Germany) JO - Chemistry VL - 12 IS - 17 N2 - Unlike traditionally used acyclic 1,2-disubstituted alkenes, the reaction of alpha,beta-unsaturated phenyl sulfones with aryl iodides under Heck reaction conditions takes place mainly by means of a four-component domino process, involving one unit of the alkene and three units of the aryl iodide, affording substituted 9-phenylsulfonyl-9,10-dihydrophenanthrenes. We report here the results of a computational study on the mechanism of this domino arylation reaction. Based on these results we can explain why vinyl sulfones, unlike other electron-deficient alkenes such as enones, preferentially follow this domino pathway instead of the usual Heck pathway. The key step is a C-H activation process in which a five-membered palladacycle is formed. The greater ability of vinyl sulfones, relative to enones, to reach the transition state that leads to the formation of the initial palladacycle makes the difference. SN - 0947-6539 UR - https://www.unboundmedicine.com/medline/citation/16596685/Understanding_sulfone_behavior_in_palladium_catalyzed_domino_reactions_with_aryl_iodides_ DB - PRIME DP - Unbound Medicine ER -