Sulphur substituted organotin compounds. Part 6. Reactions of mercaptomethyltin compounds with arenesulphenyl chlorides
β Scribed by James L. Wardell; Robin D. Taylor
- Book ID
- 104220702
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 115 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Reactions between PhaSnCHaSAr and 2-NOaCsHsSCf lead to the formation of 2-(ArSCHa)-6-NOaC,j&SSCslh,N02-2 via the [2,3] sigmatropic rearrangement of the S-arylthiosulphonium ylides EHa-S(Ar)SCaHsNOa-2. Gassman and Miura2 recently reported, in this Journal, reactions between arenesulphenyl chlorides and (methylthiomethyl)trimethylsilane, equation (1). Of particular interest was the compound X -u
π SIMILAR VOLUMES
Reports [ 1 ] have been made recently by Japanese workers on the preparation and structures of sulphi domethyl-platinum and palladium complexes, including those in which the RSCH, unit is acting as a monodentate l&and, e.g. in (PPh3)2M(CH2SMe)Cl (M = Pt and Pd) (I), and as a bidentate l&and, e.g. in
## Abstract Data presented for a range of vulcanized rubbers prepared under different conditions show that while olefinic unsaturation becomes reduced by vulcanization in the proportion of one double bond for each sulphur atom combined with a C~5~Hβunit, the original H/C ratio of 8/5 is not altered