化学
三氟甲基
丁二酰亚胺
琥珀酰亚胺
三氟甲基化
有机化学
组合化学
烷基
标识
DOI:10.1002/ejoc.201800680
摘要
Currently, a great deal of research efforts are focused on C–C bond activation for development of novel synthetic methodology. In this paper, a detrifluoroacetylation of trifluoromethyl‐β‐diketones is described, which allows for the synthesis of succinimides and 1,4‐diketones through cascade Michael addition/retro‐Claisen reaction and nucleophilic substitution/retro‐Claisen reaction. The readily available trifluoromethyl‐β‐diketones, wide substrate scope, and mild conditions make this method very practical.
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