1313867-27-4Relevant articles and documents
Gold(i)-catalyzed rearrangement of aryl alkynylaziridines to spiro[isochroman-4,2′-pyrrolines]
Kern, Nicolas,Blanc, Aurelien,Weibel, Jean-Marc,Pale, Patrick
, p. 6665 - 6667 (2011/06/25)
Alkynylaziridines carrying an aryl group could be efficiently converted to spiro[isochroman-4,2′-pyrrolines] with gold salts as catalysts. This new rearrangement involved a Friedel-Crafts type intramolecular reaction followed by cyclization of the aminoallene intermediate, both initiated by the dual σ and π Lewis acidities of gold.