Synthesis of four new carboxylic derivatives based on the [1.1.1.1]metacyclophane backbone blocked in 1,3-Alternate conformation

被引:4
|
作者
Chernova, Ekaterina F. [1 ,2 ]
Ovsyannikov, Alexander S. [2 ,3 ]
Ferlay, Sylvie [1 ]
Solovieva, Svetlana E. [2 ,3 ]
Antipin, Igor S. [2 ,3 ]
Konovalov, Alexander I. [2 ,3 ]
Kyritsakas, Nathalie [1 ]
Hosseini, Mir Wais [1 ]
机构
[1] Univ Strasbourg, Mol Tecton Lab, UMR UDS CNRS 7140, Inst le Bel, 4 Rue Blaise Pascal, F-67000 Strasbourg, France
[2] Kazan Fed Univ, Kremlevskaya Str 18, Kazan 420008, Russia
[3] Russian Acad Sci, AE Arbuzov Inst Organ & Phys Chem, Kazan Sci Ctr, Arbuzov Str 8, Kazan 420008, Russia
基金
俄罗斯基础研究基金会;
关键词
Carboxylate ligand; 1,3-Alternate conformation; Metacyclophane backbone; Ester derivatives; Suzuki coupling; STRUCTURAL-ANALYSIS; MOLECULAR TECTONICS; COORDINATION; METAL; COMPLEXATION; ALKALI; DESIGN;
D O I
10.1016/j.tetlet.2018.02.060
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Four new tetrasubstituted [1.1.1.1]metacyclophanes (4-7), that are inherently adopting a 1,3-Alternate conformation, bearing four or eight peripheral carboxylic binding sites, and appended with spacers group (alkyl or phenyl) differing by the flexibility, have been synthesised in high yields. The structures of the obtained compounds have been investigated in solution as well as in the solid state, for three of them, by using single-crystal X-ray analysis. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1377 / 1381
页数:5
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