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  Synthesis of hydroquinone-, biphenol-, and binaphthol-containing aza macroheterocycles via regioselective hydroformylation and reductive amination

Angelovski, G. (2003). Synthesis of hydroquinone-, biphenol-, and binaphthol-containing aza macroheterocycles via regioselective hydroformylation and reductive amination. Tetrahedron, 59, 8265-8274.

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Angelovski, G1, Author           
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1Department Physiology of Cognitive Processes, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497798              

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 Abstract: Rhodium(I) catalyzed regioselective hydroformylation of diolefins and subsequent reductive amination of the dialdehydes in the presence of α,ω-diamines is applied to azamacroheterocyclic ring synthesis Rhodium(I) catalyzed regioselective hydroformylation of diolefins and subsequent reductive amination of the dialdehydes in the presence of α,ω-diamines is applied to azamacroheterocyclic ring synthesis. Starting from aromatic diallyl ethers of hydroquinone, biphenol and binaphthol 20–28 membered macroheterocycles were obtained in up to 78 yield.

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 Dates: 2003
 Publication Status: Issued
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 Identifiers: BibTex Citekey: 3242
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Title: Tetrahedron
Source Genre: Journal
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Pages: - Volume / Issue: 59 Sequence Number: - Start / End Page: 8265 - 8274 Identifier: -