ChemInform Abstract: Formation and Conversion of Sulfenylhalogenides in Reactions of Halogens with 1-Phenyl-5-mercaptotetrazole and Bis(1-phenyltetrazol-5-yl)disulfide.
โ Scribed by M. A. AKHMETOV; A. I. MOVCHAN; E. G. YARKOVA; G. A. CHMUTOVA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
โฆ Synopsis
Formation and Conversion of Sulfenylhalogenides in Reactions of Halogens with 1-Phenyl-5-mercaptotetrazole and Bis(1phenyltetrazol-5-yl)disulfide. -UV and TLC studies clearly indicate, that the reaction of disulfide (I) and thiol (II) with Cl 2 and Br 2 gives the corresponding sulfenyl tetrazoles (III). An isolation of these products fails. For the different reaction mixtures, reversible as well as irreversible reactions are observed and discussed. -(AKHMETOV, M. A.; MOVCHAN, A. I.;
๐ SIMILAR VOLUMES
ฯ-Dialkylaminoalkyl Ethers of Phenyl-(5-substituted 1-phenyl-1Hpyrazol-4-yl)methanols with Analgesic and Antiinflammatory Activity. -A new series of title amino ethers (VI) (12 examples) is synthesized from alcohols (I) and examined for their biological activities. Some derivatives display good ana
Azolyl Derivatives of Nitrohalogenobutadienes. Part 2. Synthesis and Some Reactions of 1,1-Bis(3,5-dimethylpyrazol-1-yl) and 1,2,-Reaction of pentahalogenonitrobutadienes (I) with excess amounts of triazole or pyrazole (II) proceeds as electrophilic substitution of both the geminal chlorine atoms to