Journal
ORGANIC LETTERS
Volume 20, Issue 11, Pages 3430-3433Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b01407
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Funding
- CNRS
- Universite de Strasbourg
- M.R.T.
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Enamides equipped with N-acyliminium ion precursors were obtained through reduction of ynamides tethered to N-imides. Intramolecular TMSOTf-mediated trapping of N-acyliminium ions provided a variety of polyfunctionalized medium-sized diaza-heterocycles of putative pharmacological interest.
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