Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor
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Murphy, J.A. and Khan, T.A. and Zhou, S. and Mohan, M. and Thomson, D.W. (2005) Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor. Angewandte Chemie, 44 (9). pp. 1356-1360. ISSN 1521-3773 (http://dx.doi.org/10.1002/anie.200462038)
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Electron-transfer reductions of unactivated aryl and alkyl iodides with a neutral ground-state organic molecule are reported. The reducing agent 1 is formed in two steps from N-methylbenzimidazole using very simple chemistry, and subsequent treatment of the iodoalkane or -arene with 1 affords cyclized products (see scheme).
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Item type: Article ID code: 9884 Dates: DateEvent2005PublishedNotes: PV: 21365 Subjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry
Unknown DepartmentDepositing user: Strathprints Administrator Date deposited: 14 Nov 2011 11:43 Last modified: 13 Dec 2024 16:02 URI: https://strathprints.strath.ac.uk/id/eprint/9884
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