## 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 “Full Text” option. The original article is trackable v
Synthesis of novel pentacyclic pyrrolothiazolobenzoquinolinones, analogs of natural marine alkaloids
✍ Scribed by Valérie Bénéteau; Thierry Besson
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 106 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Multistep synthesis (12 steps) of new pentacyclic compounds, which are structurally very close to natural marine alkaloids, was performed via a Diels-Alder reaction between 4-methylene-5-(bromomethylene)-4,5-dihydrothiazole and a protected dioxotryptamine, itself obtained from the commercially available 2,5-dimethoxybenzaldehyde.
📜 SIMILAR VOLUMES
The synthesis of the marine pyridoacndine alkaloid merldrne (1) has been accomplished in eght steps from 25 dimethoxy-3-nitroanlllne m 9 % overall yield. 0 1997, Elsevier Science Ltd.
## 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 “Full Text” option. The original article is trackable v