## Abstract For Abstract see ChemInform Abstract in Full Text.
Annulation of Pyrrole: Application to the Synthesis of Indolizidine Alkaloids.
β Scribed by Ruth I. J. Amos; Brendon S. Gourlay; Peter P. Molesworth; Jason A. Smith; Owen R. Sprod
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 22 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
The synthesis of the racemic title alkaloid 1 has been accomplished in eight steps and 7.2% overall yield from pyrrolidine-2-thione ( ) and ethyl hex-2-enoate (6). Key steps in-
Enantiopure bicyclic 5-ethoxytetrahydropyrrolo[1,2-c]oxa-disubstituted pyrrolidines was illustrated by formal syntheses of 3,5-disubstituted indolizidine toxins, starting from 5-zol-3-one 1b was prepared in two steps from the known tosylate 4, which is readily available from (S)-pyroglutamic allylte
## Abstract For Abstract see ChemInform Abstract in Full Text.