A novel metal-free synthesis of 6H-isoindolo[2,1-α]indol-6-one
[摘要] 6 H -Isoindolo[2,1-α]indol-6-one, a core structure for a number of biologically active compounds, was synthesized in four steps. The approach is metal-free and uses a Beckmann rearrangement followed by an intramolecular cyclization.
[发布日期] [发布机构]
[效力级别] [学科分类] 内科医学
[关键词] Beckmann rearrangement;intramolecular cyclization;6H-isoindolo [2;1-a]indol-6-one [时效性]
