Title A DFT Study on the Conversion of Aryl Iodides to Alkyl Iodides: Reductive Elimination of R-I from Alkylpalladium Iodide Complexes with Accessible -Hydrogens
Authors Hao, Wei
Wei, Junnian
Chi, Yue
Walsh, Patrick J.
Xi, Zhenfeng
Affiliation Peking Univ, Coll Chem, Key Lab Bioorgan Chem & Mol Engn, BNLMS,Minist Educ, Beijing 100871, Peoples R China.
Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, 231 South 34th St, Philadelphia, PA 19104 USA.
Keywords alkylpalladium iodide complexes
computational chemistry
reaction mechanisms
reductive elimination
synthetic methods
CROSS-COUPLING REACTIONS
PALLADIUM-CATALYZED BROMOALKYNYLATION
ARYLPALLADIUM(II) HALIDE-COMPLEXES
REVERSIBLE OXIDATIVE ADDITION
BIDENTATE NITROGEN LIGANDS
BOND FORMATION
MECHANISTIC INSIGHT
EFFICIENT SYNTHESIS
EXCHANGE-REACTIONS
PD(III) COMPLEXES
Issue Date 2016
Publisher CHEMISTRY-A EUROPEAN JOURNAL
Citation CHEMISTRY-A EUROPEAN JOURNAL.2016,22,(10),3422-3429.
Abstract DFT calculations have been performed on the palladium-catalyzed carboiodination reaction. The reaction involves oxidative addition, alkyne insertion, C-N bond cleavage, and reductive elimination. For the alkylpalladium iodide intermediate, LiOtBu stabilizes the intermediate in non-polar solvents, thus promoting reductive elimination and preventing -hydride elimination. The C-N bond cleavage process was explored and the computations show that PPh3 is not bound to the Pd center during this step. Experimentally, it was demonstrated that LiOtBu is not necessary for the oxidative addition, alkyne insertion, or C-N bond cleavage steps, lending support to the conclusions from the DFT calculations. The turnover-limiting steps were found to be C-N bond cleavage and reductive elimination, whereas oxidative addition, alkyne insertion, and formation of the indole ring provide the driving force for the reaction.
URI http://hdl.handle.net/20.500.11897/435245
ISSN 0947-6539
DOI 10.1002/chem.201503910
Indexed SCI(E)
EI
PubMed
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