The iodocyclization of a series of alkenyl-substituted p-enamino esters and ketones, followed by base-promoted dehydroiodination, led to the formation of the corresponding pyrrole or tetrahydroindole derivatives. In the absence of base, the iodo-I~-enamino esters 5 and 7 underwent spontaneous aromat
✦ LIBER ✦
Formation of pyrroles from β-chloroazoalkenes and 1,3-dicarbonyl compounds
✍ Scribed by Thomas L. Gilchrist; Brian Parton; John A. Stevens
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 197 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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