Aryl radical cyclisation on to a pyrrole nucleus
โ Scribed by Keith Jones; Tim C.T. Ho; James Wilkinson
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 311 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
## Regiochemical and stereochemical evidence is presented which indicates that cobalt-mediated aryl radical cyclisations involve simple free radicals. Radical cyclisatton reactions have achieved considerable importance in synthetic chemistry'.
Abstmct: A synthesis of the te&ahydrofuro[2,3-blindole (3) in 6 step from 4-methoxyaniline involving a key cobalt-mediated aryl radical cycliin is presented. This hetuucycle is a known, late intermediate. in the synthesis of the alkaloid physovenine (2).
The 5-endo radical cyclisation of pyruvic acid derived dehydroalanines which contain chiral ester auxiliaries is reported. Cyclisation of the menthol ester derivative using Bu3SnH at 80ยฐC proceeded with low diastereoselectivity (1.