Preparative Chemistry of Chalcogenides
โ Scribed by Priv.-Doz. Dr. A. Rabenau; Dr. H. Rau
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- English
- Weight
- 155 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Extension of the reaction whereby "nucleoside dialdehydes" are cyclized by nitromethane [1,21 to nitromethane homologues [31 would be expected to produce branched nucleosides of pharmacological interest. 2-U-[(R)-Formyl-(1uracilyl)methyl] -( R )glyceraldehyde ("uridine dialdehyde") ( I ) , obtained
New azides of the type RHgN3, with R = cyclopentadienyl, cyclopropyl, and cyclopentyl, can be synthesized in this way, as can also the compound (CH&BiN3. As(CH3)3, on the other hand, like the tetraalkyl compounds of the elements of Group IV A, is inert towards CJN3; (CH&AsN3, however, can be obtaine