Organic sulfur compounds. 5. Synthesis and rearrangement of thioxanthene N-(p-tolylsulfonyl)sulfilimine
β Scribed by Tamura, Yasumitsu; Nishikawa, Yoshinori; Sumoto, Kunihiro; Ikeda, Masazumi; Murase, Masao; Kise, Masahiro
- Book ID
- 126305773
- Publisher
- American Chemical Society
- Year
- 1977
- Tongue
- English
- Weight
- 558 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
Ab initio calculations with a minimal (SI'O-3G) basis set on a number of sulfur-containing molecules are used to show that Koopmans' theorem and minimal basis calculations may be a simple but adequate way of obtaining inner-shell ionization potentials and chemical shifts of large molecules. The x-ra
1,4,5,8-Tetradeuterionaphthalene was synthesized from 1 ,Cdibromonaphthalene by two methods. In the first method naphthalene was repeatedly brominated in chloroform and then debrominated with zinc dust in alkaline deuterium oxide. In the second, 1,4-dibromonaphthaIene was nitrated to produce 1,4-dib