期刊
CHEMICAL COMMUNICATIONS
卷 47, 期 23, 页码 6665-6667出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc11351h
关键词
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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 sigma and pi Lewis acidities of gold.
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