N-substituted tetrahydro-1,3-oxazines and -oxazolidines. 2. Nitration ofN-(ω-acylamino-β,β-dinitroalkyl)tetrahydro-1,3-oxazines and -oxazolidines
✍ Scribed by A. G. Korepin; P. V. Galkin; E. K. Perepelkina; N. M. Glushakova; I. L. Eremenko; L. T. Eremenko
- Book ID
- 106521385
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 298 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The ring opening of tetrabydro-1 ,Zoxazines by nucleophilic agents, such as lithium aluminum hydride,' and bmmozincio a~&@,~ provided a useful synthetic method to fonn faminopmpanol derivatives. In our currem development of the enantioselective synthesis of (+)-rnemquinine (l), the ~p~l~nop~p~ol2 ap
## Abstract magnified image The condensation products of 2‐aminoethanol or 3‐aminopropanol (bearing an alkyl substituent on the carbon adjacent to the nitrogen) with substituted benzaldehydes proved to exist in CDCl~3~ at 300 K as threecomponent tautomeric mixtures of the diastereomeric five‐ or s