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Search for "iodoarenes" in Full Text gives 32 result(s) in Beilstein Journal of Organic Chemistry.
Recent advances in transition metal-catalyzed Csp2-monofluoro-, difluoro-, perfluoromethylation and trifluoromethylthiolation
Beilstein J. Org. Chem. 2013, 9, 2476–2536, doi:10.3762/bjoc.9.287
- readily available nucleophilic trifluoromethyl source after decarboxylation at high temperature in the presence of stoichiometric amounts of copper salts [78][79]. In 2011, Y. M. Li et al. showed that the Cu-catalyzed C–CF3 bond formation of iodoarenes could be achieved by using a sodium salt of
Hybrid super electron donors – preparation and reactivity
Beilstein J. Org. Chem. 2012, 8, 994–1002, doi:10.3762/bjoc.8.112
- , featuring pyridinylidene–imidazolylidene, pyridinylidene–benzimidazolylidene and imidazolylidene–benzimidazolylidene linkages are reported. The pyridinylidene–benzimidazolylidene and imidazolylidene–benzimidazolylidene hybrid systems were designed to be the first super electron donors to convert iodoarenes
- to aryl radicals at room temperature, and indeed both show evidence for significant aryl radical formation at room temperature. The stronger pyridinylidene–imidazolylidene donor converts iodoarenes to aryl anions efficiently under appropriate conditions (3 equiv of donor). The presence of excess
- donor as 4, while the transfer of the second electron occurs at a more negative potential than for the first electron from 1. In situ generation of 9 from 20 (1.5 equiv, Scheme 3) and reaction with iodoarenes 28 and 30 was again carried out at room temperature. As for the reactions with donor 11, the
Sonogashira–Hagihara reactions of halogenated glycals
Beilstein J. Org. Chem. 2012, 8, 675–682, doi:10.3762/bjoc.8.75
- cross-coupling reaction with iodoarenes. However, it is not only metalated sugar derivatives that have prevailed in the synthesis of C-glycosides, but also some electrophilic coupling reagents, such as glycalyl phosphates, and bromo- and iodoglycals. Glycal phosphates of type 5 were employed as
Bromine–lithium exchange: An efficient tool in the modular construction of biaryl ligands
Beilstein J. Org. Chem. 2011, 7, 1278–1287, doi:10.3762/bjoc.7.148
- the relative basicities of aryllithiums bearing methoxy, chlorine, fluorine, trifluoromethyl and trifluoromethoxy substituents at the ortho, meta, and para positions. Equilibration studies of two aryllithiums of comparable basicity with the corresponding bromo- or iodoarenes allowed them to determine
A practical microreactor for electrochemistry in flow
Beilstein J. Org. Chem. 2011, 7, 1108–1114, doi:10.3762/bjoc.7.127
- iodoarenes 8 and arenes 9 are summarized. Various yields were obtained in these experiments and not all reaction conditions were optimized. In some reactions the conversion was not complete and longer reaction times would have been necessary to achieve higher yields. Depending on the nature of the iodoarene
Donor-acceptor substituted phenylethynyltriphenylenes – excited state intramolecular charge transfer, solvatochromic absorption and fluorescence emission
Beilstein J. Org. Chem. 2010, 6, 992–1001, doi:10.3762/bjoc.6.112
- iodoarenes (Scheme 3). Compounds 1a–f were obtained as colorless solids in good yields. Derivative 1g was obtained as an orange solid in 58% yield. All compounds were purified by column chromatography and thoroughly characterized by various spectroscopic methods and analytical data. Absorption and
m-Iodosylbenzoic acid – a convenient recyclable reagent for highly efficient aromatic iodinations
Beilstein J. Org. Chem. 2007, 3, No. 19, doi:10.1186/1860-5397-3-19
- . Background In recent years, iodoarenes have gained increasing importance because they are widely used as building blocks in organic synthesis. They are particularly important as indispensable substrates for numerous methods of N-N bond formation, [1][2] for the chemistry of heterocyclic [3] and
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