<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title>IODINE  IODIDE</title><link>http://www.unboundmedicine.com/medline/ebm/research/IODINE__IODIDE</link><description>Unbound MEDLINE is a service provided by Unbound Medicine, Inc. that includes data and services from the U.S. National Library of Medicine's MEDLINE® and PubMed® databases.</description><language>en-us</language><copyright>Unbound Medicine, Inc.</copyright><item><title>Copper-Catalyzed Decarboxylative Cross-Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19894244/full_citation/Copper_Catalyzed_Decarboxylative_Cross_Coupling_of_Potassium_Polyfluorobenzoates_with_Aryl_Iodides_and_Bromides_</link><description>Shang R, Fu Y, Wang Y, et al. <br/><span class="title">Copper-Catalyzed Decarboxylative Cross-Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides. [JOURNAL ARTICLE]</span><br/><span class="source" title="Angewandte Chemie (International ed. in English)">Angew Chem Int Ed Engl 2009 Nov 5.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19894244/full_citation/Copper_Catalyzed_Decarboxylative_Cross_Coupling_of_Potassium_Polyfluorobenzoates_with_Aryl_Iodides_and_Bromides_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19894244/Copper_Catalyzed_Decarboxylative_Cross_Coupling_of_Potassium_Polyfluorobenzoates_with_Aryl_Iodides_and_Bromides_">Find Related Articles</a> </description></item><item><title>Studies on the Cl + C(2)H(5)I reaction; site specific abstraction reactions and thermodynamics of adduct formation studied by observation of HCL product.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19890528/full_citation/Studies_on_the_Cl_+_C_2_H_5_I_reaction;_site_specific_abstraction_reactions_and_thermodynamics_of_adduct_formation_studied_by_observation_of_HCL_product_</link><description>Wada R, Sharma RC, Blitz MA, et al. <br/><span class="title">Studies on the Cl + C(2)H(5)I reaction; site specific abstraction reactions and thermodynamics of adduct formation studied by observation of HCL product. [Journal Article]</span><br/><span class="source" title="Physical chemistry chemical physics : PCCP">Phys Chem Chem Phys 2009 Nov 28; 11(44):10417-26.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19890528/abstract/Studies_on_the_Cl_+_C_2_H_5_I_reaction;_site_specific_abstraction_reactions_and_thermodynamics_of_adduct_formation_studied_by_observation_of_HCL_product_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19890528/full_citation/Studies_on_the_Cl_+_C_2_H_5_I_reaction;_site_specific_abstraction_reactions_and_thermodynamics_of_adduct_formation_studied_by_observation_of_HCL_product_">Full Citation</a></description></item><item><title>Estimation of iodine intake from various urinary iodine measurements in population studies.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19888863/full_citation/Estimation_of_iodine_intake_from_various_urinary_iodine_measurements_in_population_studies_</link><description>Vejbjerg P, Knudsen N, Perrild H, et al. <br/><span class="title">Estimation of iodine intake from various urinary iodine measurements in population studies. [Journal Article, Research Support, Non-U.S. Gov't]</span><br/><span class="source" title="Thyroid : official journal of the American Thyroid Association">Thyroid 2009 Nov; 19(11):1281-6.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19888863/abstract/Estimation_of_iodine_intake_from_various_urinary_iodine_measurements_in_population_studies_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19888863/full_citation/Estimation_of_iodine_intake_from_various_urinary_iodine_measurements_in_population_studies_">Full Citation</a></description></item><item><title>Iodine/Iodide-Free Dye-Sensitized Solar Cells.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19877690/full_citation/Iodine/Iodide_Free_Dye_Sensitized_Solar_Cells_</link><description>Yanagida S, Yu Y, Manseki K <br/><span class="title">Iodine/Iodide-Free Dye-Sensitized Solar Cells. [JOURNAL ARTICLE]</span><br/><span class="source" title="Accounts of chemical research">Acc Chem Res 2009 Oct 30.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19877690/abstract/Iodine/Iodide_Free_Dye_Sensitized_Solar_Cells_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19877690/full_citation/Iodine/Iodide_Free_Dye_Sensitized_Solar_Cells_">Full Citation</a></description></item><item><title>Platinum-Catalyzed Nucleophilic Addition of Vinylsilanes at the beta-Position.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19863155/full_citation/Platinum_Catalyzed_Nucleophilic_Addition_of_Vinylsilanes_at_the_beta_Position_</link><description>Miura K, Inoue G, Sasagawa H, et al. <br/><span class="title">Platinum-Catalyzed Nucleophilic Addition of Vinylsilanes at the beta-Position. [Journal Article]</span><br/><span class="source" title="Organic letters">Org Lett 2009 Nov 5; 11(21):5066-9.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19863155/abstract/Platinum_Catalyzed_Nucleophilic_Addition_of_Vinylsilanes_at_the_beta_Position_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19863155/full_citation/Platinum_Catalyzed_Nucleophilic_Addition_of_Vinylsilanes_at_the_beta_Position_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19863155/Platinum_Catalyzed_Nucleophilic_Addition_of_Vinylsilanes_at_the_beta_Position_">Find Related Articles</a> </description></item><item><title>Visible Light Generation of Iodine Atoms and I-I Bonds: Sensitized I(-) Oxidation and I(3)(-) Photodissociation.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19848407/full_citation/Visible_Light_Generation_of_Iodine_Atoms_and_I_I_Bonds:_Sensitized_I____Oxidation_and_I_3_____Photodissociation_</link><description>Gardner JM, Abrahamsson M, Farnum BH, et al. <br/><span class="title">Visible Light Generation of Iodine Atoms and I-I Bonds: Sensitized I(-) Oxidation and I(3)(-) Photodissociation. [JOURNAL ARTICLE]</span><br/><span class="source" title="Journal of the American Chemical Society">J Am Chem Soc 2009 Oct 22.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19848407/abstract/Visible_Light_Generation_of_Iodine_Atoms_and_I_I_Bonds:_Sensitized_I____Oxidation_and_I_3_____Photodissociation_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19848407/full_citation/Visible_Light_Generation_of_Iodine_Atoms_and_I_I_Bonds:_Sensitized_I____Oxidation_and_I_3_____Photodissociation_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19848407/Visible_Light_Generation_of_Iodine_Atoms_and_I_I_Bonds:_Sensitized_I____Oxidation_and_I_3_____Photodissociation_">Find Related Articles</a> </description></item><item><title>Characteristics of the Iodide/Triiodide Redox Mediator in Dye-Sensitized Solar Cells.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19845388/full_citation/Characteristics_of_the_Iodide/Triiodide_Redox_Mediator_in_Dye_Sensitized_Solar_Cells_</link><description>Boschloo G, Hagfeldt A <br/><span class="title">Characteristics of the Iodide/Triiodide Redox Mediator in Dye-Sensitized Solar Cells. [JOURNAL ARTICLE]</span><br/><span class="source" title="Accounts of chemical research">Acc Chem Res 2009 Oct 21.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19845388/abstract/Characteristics_of_the_Iodide/Triiodide_Redox_Mediator_in_Dye_Sensitized_Solar_Cells_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19845388/full_citation/Characteristics_of_the_Iodide/Triiodide_Redox_Mediator_in_Dye_Sensitized_Solar_Cells_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19845388/Characteristics_of_the_Iodide/Triiodide_Redox_Mediator_in_Dye_Sensitized_Solar_Cells_">Find Related Articles</a> </description></item><item><title>Palladium-Catalyzed Carbonylative Cycloisomerization of gamma-Propynyl-1,3-diketones: A Concise Route to Polysubstituted Furans.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19842675/full_citation/Palladium_Catalyzed_Carbonylative_Cycloisomerization_of_gamma_Propynyl_13_diketones:_A_Concise_Route_to_Polysubstituted_Furans_</link><description>Li Y, Yu Z <br/><span class="title">Palladium-Catalyzed Carbonylative Cycloisomerization of gamma-Propynyl-1,3-diketones: A Concise Route to Polysubstituted Furans. [JOURNAL ARTICLE]</span><br/><span class="source" title="The Journal of organic chemistry">J Org Chem 2009 Oct 20.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19842675/abstract/Palladium_Catalyzed_Carbonylative_Cycloisomerization_of_gamma_Propynyl_13_diketones:_A_Concise_Route_to_Polysubstituted_Furans_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19842675/full_citation/Palladium_Catalyzed_Carbonylative_Cycloisomerization_of_gamma_Propynyl_13_diketones:_A_Concise_Route_to_Polysubstituted_Furans_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19842675/Palladium_Catalyzed_Carbonylative_Cycloisomerization_of_gamma_Propynyl_13_diketones:_A_Concise_Route_to_Polysubstituted_Furans_">Find Related Articles</a> </description></item><item><title>Axial Chirality Control During Suzuki-Miyaura Cross-Coupling Reactions: The tert-Butylsulfinyl Group as an Efficient Chiral Auxiliary.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19839613/full_citation/Axial_Chirality_Control_During_Suzuki_Miyaura_Cross_Coupling_Reactions:_The_tert_Butylsulfinyl_Group_as_an_Efficient_Chiral_Auxiliary_</link><description>Colobert F, Valdivia V, Choppin S, et al. <br/><span class="title">Axial Chirality Control During Suzuki-Miyaura Cross-Coupling Reactions: The tert-Butylsulfinyl Group as an Efficient Chiral Auxiliary. [JOURNAL ARTICLE]</span><br/><span class="source" title="Organic letters">Org Lett 2009 Oct 19.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19839613/abstract/Axial_Chirality_Control_During_Suzuki_Miyaura_Cross_Coupling_Reactions:_The_tert_Butylsulfinyl_Group_as_an_Efficient_Chiral_Auxiliary_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19839613/full_citation/Axial_Chirality_Control_During_Suzuki_Miyaura_Cross_Coupling_Reactions:_The_tert_Butylsulfinyl_Group_as_an_Efficient_Chiral_Auxiliary_">Full Citation</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19839613/Axial_Chirality_Control_During_Suzuki_Miyaura_Cross_Coupling_Reactions:_The_tert_Butylsulfinyl_Group_as_an_Efficient_Chiral_Auxiliary_">Find Related Articles</a> </description></item><item><title>A General and Efficient Approach to Aryl Thiols: CuI-Catalyzed Coupling of Aryl Iodides with Sulfur and Subsequent Reduction.</title><link>http://www.unboundmedicine.com/medline/ebm/record/19835369/full_citation/A_General_and_Efficient_Approach_to_Aryl_Thiols:_CuI_Catalyzed_Coupling_of_Aryl_Iodides_with_Sulfur_and_Subsequent_Reduction_</link><description>Jiang Y, Qin Y, Xie S, et al. <br/><span class="title">A General and Efficient Approach to Aryl Thiols: CuI-Catalyzed Coupling of Aryl Iodides with Sulfur and Subsequent Reduction. [JOURNAL ARTICLE]</span><br/><span class="source" title="Organic letters">Org Lett 2009 Oct 16.</span><br/> <a href="http://www.unboundmedicine.com/medline/ebm/record/19835369/abstract/A_General_and_Efficient_Approach_to_Aryl_Thiols:_CuI_Catalyzed_Coupling_of_Aryl_Iodides_with_Sulfur_and_Subsequent_Reduction_">Abstract</a> | <a href="http://www.unboundmedicine.com/medline/ebm/record/19835369/full_citation/A_General_and_Efficient_Approach_to_Aryl_Thiols:_CuI_Catalyzed_Coupling_of_Aryl_Iodides_with_Sulfur_and_Subsequent_Reduction_">Full Citation</a> | <a href="http://dx.doi.org/10.1021/ol902186d">Publisher Full Text</a> | <a rel="nofollow" href="http://www.unboundmedicine.com/medline/ebm/related/19835369/A_General_and_Efficient_Approach_to_Aryl_Thiols:_CuI_Catalyzed_Coupling_of_Aryl_Iodides_with_Sulfur_and_Subsequent_Reduction_">Find Related Articles</a> </description></item></channel></rss>