The 6-(aminomethyl)-2,2'-bipyridine (9c) was prepared from 6-(bromomethyl)-2,2'-bipyridine (9b) and hexamethylenetetramine followed by hydrolysis in conc. HCl solution [39]. ## ' ) For a recent discussion on the 'H-NMR consequences of this configuration, see e.g. [47].
Macrocyclic sulfamides: synthesis, hybridization, and metal binding properties
โ Scribed by Patrick D. Bailey; Anuparma Sethi; Robin G. Pritchard
- Book ID
- 104095013
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 394 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Four cyclophanes incorporating the cyclosulfamide sub-unit have been synthesised in high yield. The X-ray crystal structures of three of them, and of cyclosulfamide itself, provide useful insight into the hybridisation of such compounds. The ionophoric properties of the macrocycles are also reported, with the sulfamides showing unusual selectivity for rubidium (benzyl trimer), barium (pyridyl dimer) and silver (pyridyl dimer and trimer).
๐ SIMILAR VOLUMES
Macrocyclic receptor 1 has been synthesised, as a racemate and as a single enantiomer, utilising a Stille coupling for the formation of the biphenyl portion and a macrolactamisation as the final step. The binding properties for the racemic and the homochiral macrocycle with amino acid and dipeptide