Ring Opening of Donor-Acceptor Cyclopropanes with Acyclic 1,3-Diketones for the Synthesis of 1,6-Dicarbonyl Compounds

被引:13
|
作者
Zhang, Dongxin [1 ]
Cai, Hu [1 ]
Chen, Yan [1 ]
Yin, Lei [1 ]
Zhong, Junchao [1 ]
Zhang, Ying [1 ]
Zhang, Qian-Feng [1 ]
机构
[1] Anhui Univ Technol, Inst Mol Engn & Appl Chem, Maanshan 243002, Anhui, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 85卷 / 21期
关键词
D O I
10.1021/acs.joc.0c02290
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
1,6-Dicarbonyl compounds, representing the formal addi-tion products of the a-position of acetophenone derivatives to donor-acceptor cyclopropanes, were synthesized in two steps via first ring opening of donor-acceptor cyclopropanes with acyclic 1,3-diketones followed by DBU catalyzed retro-Claisen-type C-C bond cleavage reactions. In the first step, acyclic 1,3-diketones selectively worked as C-nucleophiles to add to donor-acceptor cyclopropanes. In the second step, the alkyl ketone part of the ring-opening products resulting from unsymmetrical 1,3-diketones was selectively cleaved in the presence of DBU in methanol.
引用
收藏
页码:14262 / 14270
页数:9
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