Studies on the Reactivity of Phenyliodonium Ylide of 2-Hydroxy-1,4-Naphthoquinone: Reactions with Indole Derivatives and Other C -Nucleophiles
β Scribed by Koulouri, Sofia; Malamidou-Xenikaki, Elizabeth; Spyroudis, Spyros; Tsanakopoulou, Maria
- Book ID
- 120336533
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 131 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The reaction of 3-substituted-4-hydroxyroxy-2H-1,2-be~othiazine 1,l-dioxides with aryl isocyanate under different equivalents of strong base NaH was studied. Seventeen of new derivatives were obtained whose structures were characterized by ' H NMR, IR, MS, elementary analysis and FeCls test. ## Key
## Abstract 1,3βDipolar cycloadditon of azomethine ylides with different dipolarophiles leads to the formation of novel heterocyclic spiro compounds having two or more chiral centers. The theoretical studies (HF/3β21G) on the 1,3βdipolar cycloaddition reaction between ethene and azomethine ylide **