Spatial structure of 4-methyl-1-(methylthiomethyl)-7-thiabicyclo[3.3.1]non-3-en-2-one

Citation
Ad. Ulendeeva et al., Spatial structure of 4-methyl-1-(methylthiomethyl)-7-thiabicyclo[3.3.1]non-3-en-2-one, PETR CHEM, 40(4), 2000, pp. 279-282
Citations number
15
Categorie Soggetti
Chemical Engineering
Journal title
PETROLEUM CHEMISTRY
ISSN journal
09655441 → ACNP
Volume
40
Issue
4
Year of publication
2000
Pages
279 - 282
Database
ISI
SICI code
0965-5441(200007/08)40:4<279:SSO4>2.0.ZU;2-1
Abstract
Disubstituted bridged thiabicyclic ketosulfide was synthesized by propanone thiomethylation with a mixture of formaldehyde, sodium methylmercaptide, a nd sodium sulfide. An X-ray diffraction study showed the six-membered heter ocycle of 4-methyl-1-(methylthiomethyl)-7-thiabicyclo[3.3.1]non-3-en-2-one to be in the chair configuration and the substituted cyclohexene ring to ha ve the sofa configuration. The dihedral angle between two plane fragments o f the molecule is equal to 68.9 degrees.