## Abstract Sulfenylchlorides, sulfenates, and sulfenamides of 1,4βnaphthoquinone were synthesized, and different methods of their syntheses were investigated. Synthesized sulfenates and sulfenamides are stable due to the large electronβwithdrawing potential of the conjugated quinonic system. Obtai
Sulfur-containing derivatives of 1,4-naphthoquinone, part 1: Disulfide synthesis
β Scribed by Maryna V. Stasevych; Maxym Yu. Plotnikov; Mykola O. Platonov; Svitlana I. Sabat; Rostyslav Ya. Musyanovych;; Volodymyr P. Novikov
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 106 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20112
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β¦ Synopsis
Disulfides of 1,4-naphthoquinone were synthesized, and different methods of their synthesis were investigated. High yields and purity of disulfides were obtained from the oxidation of thiol derivatives. The latter were prepared in high yields and purity from isothiuronic salts. The obtained disulfides are synthones for compounds with a wide spectrum of biological activity.
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