Functionalization of Benzo[b][1,6]naphthyridine Derivatives.
โ Scribed by A. S. Ivanov; N. Z. Tugusheva; L. M. Alekseeva; V. G. Granik
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 107 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Single-crystal X-ray study T = 293 K Mean '(CยฑC) = 0.009 A ร R factor = 0.043 wR factor = 0.095 Data-to-parameter ratio = 21.1 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
Enamine aus B-Dicarbonylverbindungen und Ammoniak oder primLren Aminen reagieren, wie brkannt, mit p-Benzochinon unter Bildung substituierter 5-Hydroxy-indole rl]. N, N-DialkylaminocrotonsLureester setzen sich dagegen linter analogen Redingungen direkt zuin 2,B-Dimethyl-3,7tlicarbiithoxy-benzol 1,2-
Whereas free BN radicals with unresolved ESR signals are formed on dehalogenation of pyridine-and 2-alkylpyridinedialkylchloroboranes by lithium in tetrahydrofuran 111 at 0 to 5"C, associated radicals ( I ) , whose ESR spectra show a hyperfine structure of ten lines (distances: 3.83 gauss), are obta