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ChemInform Abstract: Organic Polyvalent Iodine Compounds
ChemInform, 1996AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Viktor V. Zhdankin, Peter J. Stang
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A molecular modeling of iodinated organic compounds
Journal of Molecular Graphics and Modelling, 2021Thermodynamic quantities of some iodinated compounds have been studied by means of ab initio and density functional theory calculations. Since there are some limitations for heavy elements in the fifth row of periodic table such as the iodine atom, a high level of ab initio theory is developed to calculate the energy of iodinated compounds.
Elham Sookhaki, Mansoor Namazian
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Journal of the Chemical Society C: Organic, 1970
The use of iodine in 20% oleum for the iodination of a range of aromatic nitro-compounds is described. The conditions necessary to achieve reaction and proof of the identities of the products are included. The system has been found to behave as an electrophilic reagent but it will not introduce and iodine atom ortho to a nitro-group.
J. Arotsky, R. Butler, A. C. Darby
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The use of iodine in 20% oleum for the iodination of a range of aromatic nitro-compounds is described. The conditions necessary to achieve reaction and proof of the identities of the products are included. The system has been found to behave as an electrophilic reagent but it will not introduce and iodine atom ortho to a nitro-group.
J. Arotsky, R. Butler, A. C. Darby
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Chiral hypervalent iodine compounds
Tetrahedron: Asymmetry, 1997AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Urs H. Hirt, Thomas Wirth
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Chemischer Informationsdienst, 1977
AbstractDie Jodide (I), (IV) bzw. (VI) reagieren mit dem Reagenz J (O‐CO‐CF3)3 (II) im Molverhältnis 1:1,2 unter Konfigurationsretention zu den Substitutionsprodukten (III), (V) bzw. (VII).
M. Linskeseder, Erich Zbiral, F. Cech
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AbstractDie Jodide (I), (IV) bzw. (VI) reagieren mit dem Reagenz J (O‐CO‐CF3)3 (II) im Molverhältnis 1:1,2 unter Konfigurationsretention zu den Substitutionsprodukten (III), (V) bzw. (VII).
M. Linskeseder, Erich Zbiral, F. Cech
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Halogen Bonding in Hypervalent Iodine Compounds
2016Halogen bonds occur when electrophilic halogens (Lewis acids) attractively interact with donors of electron density (Lewis bases). This term is commonly used for interactions undertaken by monovalent halogen derivatives. The aim of this chapter is to show that the geometric features of the bonding pattern around iodine in its hypervalent derivatives ...
CATALANO, LUCA +4 more
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