Literature DB >> 19368385

Theoretical bond dissociation energies of halo-heterocycles: trends and relationships to regioselectivity in palladium-catalyzed cross-coupling reactions.

Yeimy Garcia1, Franziska Schoenebeck, Claude Y Legault, Craig A Merlic, K N Houk.   

Abstract

Selectivity of the palladium-catalyzed cross-coupling reactions of heterocycles bearing multiple identical n class="Chemical">halogens is mainly determined by the relative ease of oxidative addition. This is related to both the energy to distort the carbon halogen bond to the transition-state geometry (related to the CX bond-dissociation energy) and to the interaction between the heterocycle pi* (LUMO) and PdL(2) HOMO (J. Am. Chem. Soc. 2007, 129, 12664). The computed bond dissociation energies of a larger series of halo-heterocycles have been explored with B3LYP and higher accuracy G3B3 calculations. Quantitative trends in bond dissociation energies have been identified for five- and six-membered chloro and bromo substituted heterocycles with N, O, and S heteroatoms.

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Year:  2009        PMID: 19368385      PMCID: PMC2730358          DOI: 10.1021/ja9004927

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  11 in total

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5.  Origin of regioselectivity in palladium-catalyzed cross-coupling reactions of polyhalogenated heterocycles.

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10.  SUZUKI-MIYAURA COUPLING REACTIONS OF 3,5-DICHLORO-1,2,4-THIADIAZOLE.

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