Synthesis and structure of a chiral areno-bridged [2.4]metacyclophane

Abstract : The reductive coupling reaction of 1,4-bis(3-acetyl-5-tert-butyl-2-methoxyphenyl)butane 3 was carried out using TiCl4-Zn in pyridine followed by a McMurry coupling reaction to afford the compounds anti and syn 1,2-dimethyl[2.4]MCP-1-ene 4. Bromination of 4 with BTMA-Br$_3$ in dry CH$_2$Cl$_2$ afforded the interesting compound 1,2-bis-(bromomethyl)-5,15-di-tert-butyl-8,18-dimethoxy[2.4]MCP-1-ene 6 and consecutive debromination with Zn and AcOH in CH2$_C$l$_2$ solution afforded the stable solid 5,15-di-tert-butyl-8,18-dimethoxy-1,2-dimethylene[2.4]MCP 7 in 89% yield. Compound 7 was conveniently employed in a Diels–Alder reaction with dimethyl acetylenedicarboxylate (DMAD) to provide 2-(3′,6′-dihydrobenzo)-5,15-di-tert-butyl-8,18-dimethoxy[2.4]MCP-4′,5′-dimethylcarboxylate 8 in good yield. Diels–Alder adduct 8 was converted into a novel and inherently chiral areno-bridged compound [2.4]MCP 9 by aromatization. The chirality of the two conformers was characterized by circular dichroism (CD) spectra of the separated enantiomer which are perfect mirror images of each other.
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Dernière modification le : jeudi 1 février 2018 - 01:39:30


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Thamina Akhter, Md. Monarul Islam, Taisuke Matsumoto, Junji Tanaka, Pierre Thuéry, et al.. Synthesis and structure of a chiral areno-bridged [2.4]metacyclophane. Tetrahedron, Elsevier, 2017, 74, pp.329-335. 〈〉. 〈10.1016/j.tet.2017.11.075〉. 〈cea-01656007〉



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