887616-85-5Relevant academic research and scientific papers
Direct nucleophilic acylation of nitroalkenes promoted by a fluoride anion/thiourea combination
Mattson, Anita E.,Zuhl, Andrea M.,Reynolds, Troy E.,Scheldt, Karl A.
, p. 4932 - 4933 (2007/10/03)
The direct nucleophilic acylation of nitroalkenes is reported utilizing a fluoride-initiated rearrangement of protected thiazolium carbinols. The key combination of fluoride anion and thiourea accesses carbonyl anion reactivity without the use of amine or
