Chiral synthesis of (+)-eburnamine, (–)-eburnamenine, and (–)-eburnamonine
- 1 January 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 2,p. 305-309
- https://doi.org/10.1039/p19850000305
Abstract
The (S)-trityl-lactone (6), easily prepared from L-glutamic acid or D-mannitol, has been stereo-selectively converted into (+)-eburnamine (3), (–)-eburnamenine (4), and (–)-eburnamonine (2), via the dithiane-lactone (15).This publication has 2 references indexed in Scilit:
- Synthesis of vinca alkaloids and related compounds—XVITetrahedron, 1983
- Synthesis and reduction of pentacyclic immonium salts. Application to the synthesis of (.+-.)-(E)-norvincamoneThe Journal of Organic Chemistry, 1980