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Here, we demonstrate a fundamentally new reactivity of the silyl enol ether functionality utilizing an in situ-generated iodonitrene-like species. The present transformation inserts a nitrogen atom between the silyl enol ether olefinic carbons with the concomitant cleavage of the C═C bond. Overall, this facile transformation converts a C-nucleophilic silyl enol ether to the corresponding C-electrophilic
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Lin et al. (Tue,) studied this question.
www.synapsesocial.com/papers/68e6012eb6db643587594d99 — DOI: https://doi.org/10.1021/jacs.4c07111
Alex W. H. Lin
Arghya Ghosh
Simon Yellen
Journal of the American Chemical Society
Rice University
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