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Synthesis 2020; 52(21): 3153-3161
DOI: 10.1055/s-0040-1707175
DOI: 10.1055/s-0040-1707175
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Remote Deprotometalation-Iodolysis of N,N-Diisopropyl-2-trimethylsilylferrocenecarboxamide: A New Route Toward 1,1′-Disubstituted Ferrocenes
This work was supported by the Université de Rennes 1 and CNRS.Further Information
Publication History
Received: 19 May 2020
Accepted after revision: 08 June 2020
Publication Date:
01 July 2020 (online)
Abstract
The 1,1′-disubstitution is currently the most frequent substitution pattern encountered in the ferrocene series. Here an original access based on the remote deprotometalation of N,N-diisopropyl-2-trimethylsilylferrocenecarboxamide is reported. The key intermediate, 1′-iodo-N,N-diisopropylferrocenecarboxamide, was prepared in multiple grams and was further functionalized toward fifteen 1′-substituted iodoferrocenes.
Key words
ferrocene - 1,1′-disubstitution - carboxamide - remote functionalization - functional group manipulationSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0040-1707175.
- Supporting Information
- CIF File
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