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Lewis Acid Enables Ketone Phosphorylation to Form a C–P Bond and a C–C Bond: Synthesis of 9-Phosphoryl Fluorene Derivatives
Organic Letters ( IF 4.9 ) Pub Date : 2021-08-26 , DOI: 10.1021/acs.orglett.1c02504
Xiao-Hong Wei 1 , Chun-Yuan Bai 1 , Ai-Jun Wang 1 , Qiao-Liang Feng 1 , Lian-Biao Zhao 1 , Ping Zhang 1 , Zhen-Hua Li 1 , Qiong Su 1 , Yan-Bin Wang 1
Affiliation  

An efficient method for the Lewis acid promotion of the synthesis 9-phosphoryl fluorenes has been reported. This method focuses on ketone phosphonylation to form a C–P bond and a C–C bond between diphenylmethanone and H-phosphinate esters, H-phosphites, and H-phosphine oxides via phospha-aldol elimination, in which a series of 9-phosphoryl fluorene derivatives were selectively obtained in moderate to excellent yields.

中文翻译:

路易斯酸使酮磷酸化形成 C-P 键和 C-C 键:9-磷酰基芴衍生物的合成

已报道了一种用于路易斯酸促进合成 9-磷酰基芴的有效方法。该方法侧重于酮膦酰化,通过磷醛醇消除在二苯甲酮和 H-次膦酸酯、H-亚磷酸酯和 H-氧化膦之间形成 C-P 键和 C-C 键,其中一系列 9-磷酰基以中等至极好的收率选择性地获得芴衍生物。
更新日期:2021-09-17
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