Alkylation reactions of hydantoins and succinimides
โ Scribed by D. K. Yung; T. P. Forrest; M. L. Gilroy; M. M. Vohra
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 463 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0022-3549
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๐ SIMILAR VOLUMES
The analysis of hydantoin and succinimide anticonvulsants was carried out using techniques of chemical ionization and collision activated dissociation (CAD) in a quadrupole ion trap. Dimethyl ether was used as the chemical ionization reagent gas to generate [M + HI+ and IM + 13)' products, with the
## Abstract Of the isoelectronic 6โelectron systems **1a, 1b, 1c** __(Table 1)__ the deprotonated amides **2** might be useful derivatives for amine acidification (eq. (1)) if the carbonyl group is __sterically protected__ as shown in **3**. The tetrasubstituted succinimides **4, 5, 7, 8** and **9*
## Abstract We have examined the reaction of hydantoin (=imidazolidineโ2,4โdione) with (formylphenyl)boronic acids, where the addition of a boronic acid group is hoped to increase bioactivities. Addition of (2โformylphenyl)boronic acid to hydantoin gave an unexpected azaborine compound, which presu