This is the authors' abstract. We don't add key points for this paper.
A new Passerini-type reaction in which hexafluoroisopropanol functions as the acid component is reported. The reaction tolerates a broad range of isocyanides and aldehydes, and the formed imidates can be reduced toward β-amino alcohols under mild and metal-free conditions. In addition, the imidate products were shown to undergo an unprecedented retro-Passerini-type reaction under microwave conditions, providing valuable mechanistic information about the Passerini reaction and its variations.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Saya et al. (2018) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: