The contrasting comformational behaviour of 5-aryl-5-methyl-1,3-dioxanes and 1-aryl-1-methylcyclohexahes
โ Scribed by Michael J. Cook; Khalida Nasri; Sunil M. Vather
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 123 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
tie chair + chair equilibrium of 5-aryl-5-methyl-1,3-dioxanes, unlike that of 1-aryl-I-methylcyclohexanes, is remarkably sensitive to the nature of substituents on the aromatic ring.
An interaction involving the the arcmatic group and the dioxane oxygen atoms or C-O bonds is proposed.
๐ SIMILAR VOLUMES
Pentaerythritol, (1,1,1-trishydroxymethyl)methyl methane and (1,1,1-trishydroxymethyl)nitromethane are converted into 2-aryl-5,5-bis(hydroxymethyl), 2-aryl-5-hydroxymethyl-5-methyl-or 2-aryl-5-hydroxymethyl-5-nitro-1,3-dioxanes and a range of derivatives. X-Ray and NMR analysis establishes that the
## Abstract magnified image magnified image The synthesis of a new set of selenadiazoles, 4โarylโ5โ(1โarylโ2โmethylโ2โnitropropyl)โ1,2,3โselenadiazoles (**4**) derived from 2โ[4โmethylโ4โnitroโ1,3โdiarylpentylidene]โ1โhydrazinecarboxamide (**3**) has been reported. THF has been found to be the so