Pyrrolizidine synthesis by intramolecular cyclization of a substituted azacyclooctane-4,5-oxide
✍ Scribed by Richard S. Glass; Donald R. Deardorff; Lawrence H. Gains
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 216 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Pyrrolizidine alkaloids have been isolated from a variety of plant families.' In addition they have been found in several species of butterflies and moths2 and in a millipede.3 The pharmacology of these alkaloids has been studied extensively 134 and dangers to human health recognized. 4b,5 Recently, a number of synthetic results to the pyrrolizidine ring system (l-azabicyclo [3.3.0] octane) have been published.6 A transannular route to this ring system has been communicated' and also used8 in a synthesis of hemiloline la as described in the accompanying paper.
In view of these results our related independent work is presented here.
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