## Abstract The stereochemistry in solution of three octathia[2.2.2.2]metacyclophanes has been investigated by means of ^1^H NMR spectroscopy. The results lead to the conclusion that the saddle or crown conformation is preferred for these compounds, depending on the substitution pattern of the cons
Synthesis and conformational behaviour of 1,9,17-triaza[2.2.2]metacyclophane-2, 10, 18-trione derivatives
โ Scribed by Farouk Eltayeb Elhadi; W. David Ollis; J. Fraser Stoddart; David J. Williams; Kwamena A. Woode
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 258 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The 1,9, 17 -triaza[2 2.21 metacyclophane-2, 10, 18-trlone derlvatlves (1) -( 2) have been synthesised
X-Ray crystallography shows that the 1,9, 17trimethyl derivative (3) adopts a Crown conformation (11) m the solid state. n m r. spectroscopy lndlcates that both the 1, 9-dlmethyl-17-benzyl-
(2) and
๐ SIMILAR VOLUMES
Tetrahydroxy[2.2] metacyclophanes are formed via the aluminium mediated pinacol coupling reaction of 1,3-benzenedicarboxaldehydes. The results indicate that the presence of functional groups in the aromatic ring of the dialdehydes plays an important role in the formation of the cyclophane structure
## Abstract Baseโcatalyzed condensation of 1,2โbis[5โ__tert__โbutylโ3โ(5โ__tert__โbutylsalicyl)โ2โhydroxyphenyl]ethane (8) with formaldehyde in xylene affords a novel ethyleneโbridged calixareneโanalogous macrocyclic metacyclophane. However, not the desired 2 has been obtained. Instead, the novel m