2001
DOI: 10.1039/b102749m
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Synthesis of imines, diimines and macrocyclic diimines as possible ligands, in aqueous solution

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Cited by 76 publications
(59 citation statements)
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References 38 publications
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“…Dialdehyde [1,2-bis(2-carboxyaldehydephenoxy)-ethane] used as the precursor, was synthesized according to the reported method [34]. Novel lariat ethers were synthesized by following the previous procedure [35] and characterized as follows.…”
Section: Synthesismentioning
confidence: 99%
“…Dialdehyde [1,2-bis(2-carboxyaldehydephenoxy)-ethane] used as the precursor, was synthesized according to the reported method [34]. Novel lariat ethers were synthesized by following the previous procedure [35] and characterized as follows.…”
Section: Synthesismentioning
confidence: 99%
“…More than a decade ago, we have developed an interesting protocol for the synthesis of Schiff bases in which the condensation process was performed in a less expected solvent for this purpose, that is water [1,2]. By using this aqueous imine synthesis protocol, we planned to perform the synthesis of recalcitrant diimines 1, starting from low-reactivity carbonyl compounds and aliphatic diamines (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%
“…16 We noticed from the literature that imines can be conveniently prepared in pure water without the presence of a catalyst from corresponding amines and aldehydes. 17 Since we were interested in preparing imidazolidines in a fast and easy way, we wanted therefore to investigate, if it would be also possible to prepare aminals in a similar way. So far aminals have never been synthesized and isolated in pure water.…”
Section: Introductionmentioning
confidence: 99%