Thermischer Zerfall isomerer Dihydro-1,3,4-thiadiazol-1,1-dioxide1)
β Scribed by Quast, Helmut ;Kees, Frieder
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1981
- Tongue
- English
- Weight
- 287 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0009-2940
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π SIMILAR VOLUMES
We have performed a product and kinetic study of the hydrolysis of 3,4-diphenyl-1,2,5-thiadiazole-1,l-dioxide in aqueous solution. Benzil and sulfamide are the only products of hydrolysis and are formed in equimolar yields. The kinetic results indicate that a first order law is followed up to 90% c
An on-column HPLC procedure using a chiral stationary phase (CSP) was developed for the determination of rate constants and free energy barriers of enantiomerization of (+/-)IDRA21. Subsequently, the HPLC method was applied for investigation of two structurally related chiral compounds. The individu