6533b828fe1ef96bd12882b5
RESEARCH PRODUCT
Sequential Nucleophilic−Electrophilic Reactions Selectively Produce Isomerically Pure Nona‐ B ‐Substituted o ‐Carborane Derivatives
Clara ViñasFrancesc TeixidorReijo SillanpääGemma BarberàRaikko Kivekässubject
010405 organic chemistryChemistrychemistry.chemical_element010402 general chemistryIodine01 natural sciences0104 chemical sciences3. Good healthInorganic ChemistryReaction sequenceNucleophileElectrophileCarboraneOrganic chemistryBorondescription
Nine equal substituents on the intensively studied o-carborane have been obtained for the first time by a combined nucleophilic-electrophilic reaction sequence. Iodine and methyl groups have been introduced to prove the generality of the method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2003-04-01 | European Journal of Inorganic Chemistry |