Synthesis of 2-(3-indolyl)-1,4-naphthoquinones using 3-iodoindoles
โ Scribed by Yasuhiro Tanoue; Moritsugu Hamada; Norihisa Kai; Kazunori Sakata; Mamoru Hashimoto; Takeshi Nagai
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 92 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
The usefulness of 3-iodoindoles available for introduction of an indole unit is presented. The reaction of various halo-3-iodoindoles with 1,4-naphthoquinone gave the corresponding 2-(3-indolyl)-1,4-naphthoquinones in moderate yields. The 3-iodoindole was used for synthesis of a compound containing both naphthazarin and indole skeletons.
๐ SIMILAR VOLUMES
## Abstract magnified image The usefulness of 3โiodoindole available for introduction of an indole unit is presented. The reaction of 3โiodoindole with 2โbromo(or methyl)โ1,4โnaphthoquinone in acetic acid gave 2โbromo(or methyl)โ3โ(3โindolyl)โ1,4โnaphthoquinone. On the other hand, the reaction of 3
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
Synthesis of 2-Alkoxy-3-ethoxythiocarbonylthio-1,4-naphthoquinones -[by reaction of 2,3-dichloronaphthoquinone (I) with dithiocarbonate (II) in alcoholic media]. -(CHERNILEVSKAYA, G. S.; STADNITSKAYA, N. E.;