AbstractÐDiels±Alder reactions between 2-or 3-vinylpyrrolo[2,3-b]pyridine with various dienophiles were investigated. The pyrido[2,3b]indole adducts 9 and 13 obtained led us to the preparation of potential cytotoxic agents 19 and 20.
Synthesis, alkylation, and structural studies of 2-vinylpyrrolo[1,2-a]indoles
✍ Scribed by N. Z. Tugusheva; S. Yu. Ryabova; N. P. Solov'eva; V. G. Granik
- Publisher
- Springer US
- Year
- 1994
- Tongue
- English
- Weight
- 876 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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
Synthetic approaches toward mitomyoins (I) (1) have been made energetically by a Lederle group snd the synthesis of 7-methoxymitosene (II) was reported (2). However, their various
## Mitomycin antibiotics (I) have a novel ring system that is aziridinopyrrolo II 1,2-a indoloquinone(1). In synthetic studies on mitomycin analogs Lederle group synthesised 7-benzyloxy-9H-pyrrolo 1,2-a indole(2) and substituted 2,3r.