| | 1 | Author
| Teresa Borowiak3, Irena Wolska3, Herbert Mayrb, Janusz Baranc | Requires cookie* | | | Title
| X-Ray Structure4]non-2-ene  | | | | Abstract
| of 6(is)-[2(Z)-(Hydroxyimino)-2-phenylethyIidene]-7,7,8,8,9,9-hexamethyl-3-phenyl-l,2-oxazaspiro[4. The X-ray crystallographic structure of the title compound, a product of a 1,3-dipolar cy cloaddition reaction of benzonitrile oxide to 3,3,4,4,5,5-hexamethyl-l,2-bis(methylene)cyclo-pentane, has been determined. Colourless plates crystallize in the orthorhombic space group Pbca with cell dimensions a = 13.698(2), b = 11.836(2), c = 29.157(4) A, V= 4727.2(1.2)A3, Z = 8, 3736 reflections, final R(F) = 0.063 and wR(F2) = 0.166. The crystals are racemic, the molecules of opposite chirality form centrosymmetric dimers via intermolecular hydro gen bonds O-H -N between their oxime groups. The molecules are highly strained and the geometrical consequences of the steric strain are discussed. | | | |
Reference
| Z. Naturforsch. 56b, 354—358 (2001); received November 27 2000 | | | |
Published
| 2001 | | | |
Keywords
| 1, 3-Dipolar Cycloaddition Product, Oxime, Isoxazoline | | | |
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| default:Reihe_B/56/ZNB-2001-56b-0354.pdf | | | | Identifier
| ZNB-2001-56b-0354 | | | | Volume
| 56 | |
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